COZART EIA COCAINE ORAL FLIUD KIT

{0}------------------------------------------------ K030234 # PREMARKET NOTIFICATION [510(k)] SUMMARY # APR 2 8 2003 | Submitter | Cozart Bioscience Ltd<br>45 Milton Park<br>Abingdon<br>Oxfordshire OX14 4RU<br>UK<br>Tel No: 01235 861483<br>Fax No: 01235 835607 | |----------------|-----------------------------------------------------------------------------------------------------------------------------------| | Contact Person | Dr Roberto Liddi<br>Quality Assurance & Regulatory Affairs Manager | | Date | 20th January 2003 | | Device Name | Cozart EIA Cocaine Oral Fluid Kit | Trade Name Cozart EIA Cocaine Oral Fluid Kit Classification Name Cocaine Test System Classification Class II Code of Federal Regulations Title 21 Food and Drugs Part 862 Clinical Chemistry and Clinical Toxicology Devices Subpart D Clinical Toxicology Test Systems 862.3250 Cocaine and cocaine metabolite test system Establishment Registration No 3002336046 Performance Standards BS EN ISO 9001:1994; EN 46001:1996 Substantial Equivalence STC Opiates Micro-Plate EIA (Orasure® Application), 510(k) no. K981341 {1}------------------------------------------------ | Parameter | Cozart EIA Cocaine Oral Fluid Kit | Cocaine Metabolite Micro-Plate EIA<br>(Orasure® Application), 510(k) no.<br>K982061 | |-------------------|---------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|------------------------------------------------------------------------------------------------------------------------------------| | Intended Use | Qualitative test for Cocaine in human oral<br>fluid with a 30ng/ml cutoff. Recommend<br>confirmation of positive results by GC/MS. | Qualitative test for Cocaine in human oral<br>fluid with a 10ng/ml cutoff. Recommend<br>confirmation of positive results by GC/MS. | | Target Population | Clinical and forensic samples. | Clinical samples. | | Design | Competitive ELISA | Competitive ELISA | | Enzyme | Horse Radish Peroxidase | Horse Radish Peroxidase | | Results | Read spectrophotometrically at 450nm. | Read spectrophotometrically at 450nm. | | Calibrators | 0, 5, 10, 50ng/mL | 0, 5, 10, 50ng/mL | | Matrix | Human Oral Fluid | Human Oral Fluid | | Controls | None supplied but Cozart recommends<br>using external controls. | Unknown | | Method Comparison | 177 samples were tested, 100 screened<br>positive for cocaine and metabolites, of<br>which 100 were confirmed positive by<br>GC/MS. 77 samples screened negative for<br>cocaine and metabolites and 71 were<br>confirmed negative by GC/MS. | 92% Agreement as compared to GC/MS | | Precision | CV (%) of 1.9 – 10.7% | CV (%) of 5 – 11.2% | | Sensitivity | 1.8ng/mL | <5ng/mL | | Specificity | 29 potential interferents tested – none<br>cross-reacted | Unknown | # Introduction The Cozart EIA Cocaine Oral Fluid Kit is a laboratory based test for the detection of cocaine and metabolites in human oral fluid using a cutoff equivalent to 30ng/mL. The device detailed above was compared to Gas Chromatography/Mass Spectrometry (GC/MS). Cozart Bioscience Ltd is the manufacturer of the Opiates Oral Fluid Kit. We have not purchased this device from another manufacturer and the device is not marketed under another product name. # Intended Use The Cozart EIA Cocaine Oral Fluid Kit is intended for use in clinical and forensic laboratories when used in conjunction with the Cozart RapiScan Oral Fluid collection system. Using this collection system it provides qualitative screening results for cocaine and metabolites in human oral fluid at a cutoff concentration of 10ng/ml. This is equal to 30ng/mL in undiluted oral fluid as the collection system involves a 1:3 dilution of the sample. The remainder of this document will refer to the 10ng/mL cutoff concentration. This assay is for professional use only and provides only a preliminary analytical test result. Clinical consideration and professional judgement must be applied to any drug of abuse test result, particularly in evaluating a preliminary positive {2}------------------------------------------------ result. In order to obtain a more confirmed analytical result a more specific alternative chemical method is needed. Gas Chromatography/Mass Spectrometry (GC/MS) is the preferred confirmatory method. #### Target Population The target population for the Cozart EIA Cocaine Oral Fluid Kit is clinical and forensic samples. #### Where Used The Cozart EIA Cocaine Oral Fluid Kit is designed for use in clinical and forensic laboratories. For professional use only. # Design As can be seen from the Principle of the Test section in the pack insert, the Cozart EIA Cocaine Oral Fluid Kit is a competitive ELISA for the detection of cocaine and its metabolites in human oral fluid. # Materials The Cozart EIA Cocaine Oral Fluid kit supplies the following reagents - a microtitre plate coated with antibody, enzyme conjugate reagent, wash buffer, substrate solution, stop solution and four calibrators (0, 5, 10 and 50ng/ml benzoylecgonine in oral fluid matrix). # Performance #### Method Comparison Cocaine Oral Fluid The Cozart EIA Kit was compared to Gas Chromatography/Mass Spectrometry (GC/MS). All the samples were tested with the Cozart EIA Cocaine Oral Fluid Kit according to the pack insert enclosed. 177 samples were tested through the Cozart EIA Cocaine Oral Fluid Kit, 100 screened positive and 100 were confirmed positive by GC/MS. 77 samples screened negative and 71 were confirmed negative by GC/MS. Of the 177 samples tested 15 were between -50% cutoff and +50% cutoff. | New Device | GC/MS<br>Negs | Near Cutoff<br>GC/MS<br>Negs * | Near Cutoff<br>GC/MS<br>Pos ** | GC/MS<br>Pos*** | Percent Agreement<br>with<br>GC/MS | |------------|---------------|--------------------------------|--------------------------------|-----------------|------------------------------------| | Pos<br>100 | 0 | 0 | 4 | 100 | 100 | | Neg<br>77 | 71 | 6 | 5 | 6 | 92 | * Between -50% Cutoff and the Cutoff. ** Between +50% Cutoff and the Cutoff. *** Total number of positives (includes near cutoff samples). 96% overall agreement as compared with GC/MS Cozart EIA Cocaine Oral Fluid Kit {3}------------------------------------------------ # Precision The precision obtained for the Cozart EIA Cocaine Oral Fluid Kit produced CVs less than 9%. The total precision for the kit produced CVs less than 11%. The Cozart EIA Cocaine Oral Fluid Kit is a qualitative manual ELISA assay and CVs of less than 10% are acceptable for this assay type. #### Sensitivity The sensitivity of the Cozart EIA Cocaine Oral Fluid Kit is 1.8ng/ml. # Specificity Twenty-nine potentially interfering unrelated substances were tested for cross reactivity in the Cozart Cocaine Oral Fluid Kit and none were found to cross react. Four related compounds were tested and three showed a level of cross reactivity. #### Cutoff Concentration Testing samples at the cutoff concentration, 50% above and 50% below were carried out to validate the cutoff concentration. The absorbances obtained for the 5ng/ml sample were all higher than the 10ng/ml cutoff calibrator. Similarly the absorbances obtained for the 15ng/ml sample were all lower than the 10ng/ml cutoff calibrator. #### Interference Studies A range of parameters including alcohol, sample adequacy indicator dye, haemoglobin, smoking, coffee, tea, water, food, orange juice, hard candy, chewing gum and mouthwash were tested for interference in the Cozart Cocaine Oral Fluid Kit. No interference was observed with any of the parameters. #### Stopped Assay Stability The stability of the stopped assay was investigated by reading the absorbance at 450nm at times 0, 5, 10, 15, 30, 45 and 60 minutes. The Cozart EIA Cocaine Oral Fluid Kit must be read within 15 minutes at 450mm. #### Assay Drift Sample addition at time 0, 2.5, 5, 7.5, 10, 12.5, 15, 17.5, 20, 22.5 and 25 minutes was investigated. Little change was observed across the plate and therefore sample addition to a Cozart EIA Cocaine Oral Fluid Kit must take place within 25 minutes. {4}------------------------------------------------ Image /page/4/Picture/1 description: The image shows the logo for the U.S. Department of Health & Human Services. The logo consists of a stylized caduceus symbol, which is a staff with two snakes coiled around it, and the text "DEPARTMENT OF HEALTH & HUMAN SERVICES - USA" arranged in a circular fashion around the symbol. The logo is black and white. APR 2 8 2003 Food and Drug Administration 2098 Gaither Road Rockville MD 20850 Dr. Roberto Liddi Quality Assurance & Regulatory Affairs Manager Cozart Bioscience Ltd 45 Milton Park Abingdon Oxfordshire OX14 4RU UK Re: k030234 Trade/Device Name: Cozart EIA Cocaine Oral Fluid Kit Regulation Number: 21 CFR 862.3250 Regulation Name: Specimen transport and storage container Regulatory Class: Class II Product Code: DIO Dated: April 15, 2003 Received: April 18 2003 Dear Dr. Liddi: We have reviewed your Section 510(k) premarket notification of intent to market the device referenced above and have determined the device is substantially equivalent (for the indications for use stated in the enclosure) to legally marketed predicate devices marketed in interstate commerce prior to May 28, 1976, the enactment date of the Medical Device Amendments, or to devices that have been reclassified in accordance with the provisions of the Federal Food. Drug, and Cosmetic Act (Act) that do not require approval of a premarket approval application (PMA). You may, therefore, market the device, subject to the general controls provisions of the Act. The general controls provisions of the Act include requirements for annual registration, listing of devices, good manufacturing practice, labeling, and prohibitions against misbranding and adulteration. If your device is classified (see above) into either class II (Special Controls) or class III (PMA), it may be subject to such additional controls. Existing major regulations affecting your device can be found in Title 21, Code of Federal Regulations (CFR), Parts 800 to 895. In addition, FDA may publish further announcements concerning your device in the Federal Register. Please be advised that FDA's issuance of a substantial equivalence determination does not mean that FDA has made a determination that your device complies with other requirements of the Act or any Federal statutes and regulations administered by other Federal agencies. You must comply with all the Act's requirements, including, but not limited to: registration and listing (21 CFR Part 807); labeling (21 CFR Parts 801 and 809); and good manufacturing practice requirements as set forth in the quality systems (QS) regulation (21 CFR Part 820). {5}------------------------------------------------ Page 2 - This letter will allow you to begin marketing your device as described in your Section 510(k) premarket notification. The FDA finding of substantial equivalence of your device to a legally marketed predicate device results in a classification for your device and thus, permits your device to proceed to the market. If you desire specific information about the application of labeling requirements to your device, or questions on the promotion and advertising of your device, please contact the Office of In Vitro Diagnostic Device Evaluation and Safety at (301) 594-3084. Also, please note the regulation entitled, "Misbranding by reference to premarket notification" (21CFR Part 807.97). You may obtain other general information on your responsibilities under the Act from the Division of Small Manufacturers, International and Consumer Assistance at its toll-free number (800) 638-2041 or (301) 443-6597 or at its Internet address http://www.fda.gov/cdrh/dsma/dsmamain.html. Sincerely yours, Steven Butman Steven I. Gutman, M.D., M.B.A. Director Office of In Vitro Diagnostic Device Evaluation and Safety Center for Devices and Radiological Health Enclosure {6}------------------------------------------------ Page 1 of 510(k) Number (if known): K 030 Z3 4 Device Name:__________________________________________________________________________________________________________________________________________________________________ Cozart EIA Cocaine Oral Fluid Kit Indications For Use: The Cozart EIA Cocaine Oral Fluid Kit is intended for use in clinical and analytical laboratories when used in conjunction with the Cozart RapiScan Oral Fluid collection system. Using this collection system it provides qualitative screening results for cocaine and metabolites in human oral fluid at a cutoff concentration of 10ng/ml. This is equal to 30ng/ml. in undiluted oral fluid as the collection system involves a 1:3 dilution of the sample. This assay is for professional use only and provides only a preliminary analytical test result. Clinical consideration and professional judgement must be applied to any drug of abuse test result, particularly in evaluating a preliminary positive result. In order to obtain a more confirmed analytical result a more specific alternative chemical method is needed. Gas Chromatography/Mass Spectrometry (GC/MS) is the preferred confirmatory method. Sean Cooper Division Sign-Off) Clinical Labora 510(k) Number K 030234 (PLEASE DO NOT WRITE BELOW THIS LINE-CONTINUE ON ANOTHER PAGE IF NEEDED) Concurrence of CDRH, Office of Device Evaluation (ODE) Ry (Optional Format 3-10-98)