RAPIDONE-ECSTASY TEST

{0}------------------------------------------------ # NOV 2 6 2001 K013180 ### 510(k) Summary #### Submitter's Name/Address: American Bio Medica Corporation 122 Smith Road Kinderhook, NY 12106 Date of Preparation of this Summary: #### Device Trade or Proprietary Name: Device Common/Usual Name or Classification Name: #### Contact Person: Henry Wells VP Product Development Phone: 518 758 8158 518-758 8171 Fax: September 21, 2001 'RapidOne'-Ecstasy' Test MDMA test system Classification Number/Class [no classification regulation]/ClassII This 510(k) Summary is being submitted in accordance with the requirements of 21 CFR 807.92. The assigned 510(k) number is: _ HO13180 Predicate Device: MedTox Diagnostics, Inc., Verdict II-Methamphetamine Test. (510(k) No. K-010226). #### Test Description: The assay employed in the 'RapidOne'-Ecstasy' Test is based on the same principle of highly specific reaction between antigens and antibodies. This assay is a one-step, immunoassay in which a specially labeled drug (drug conjugate) competes with drug that may be present in the sample for the limited number of binding sites on the antibody. The test device consists of a membrane strip onto which a drug conjugate has been immobilized. A colloidal gold-antibody complex is dried at one end of a membrane. In the absence of any drug in the urine sample, the colloidal goldantibody moves with the urine by capillary action to contact the immobilized drug conjugate. An antibody-antigen reaction occurs forming a visible line in the 'test' area. The formation of a visible line in the 'test' area occurs when the test is negative. When drug is present in the urine sample, the drug or metabolite will compete with the immobilized drug conjugate in the test area for the limited antibody sites on the colloidal gold-antibody complex. If sufficient amount of drug is present, it will fill all of the available binding sites, thus preventing attachment of the labeled antibody to the drug {1}------------------------------------------------ conjugate. An absence of a color band (line) in the 'test' area is indicative of a positive result. A control band (line), comprised of a different antibody/antigen reaction, is present on the membrane strip. The 'control; line is not influenced by the presence or absence of drug in the urine, and therefore, should be present in all reactions. #### Intended use: "RapidOne'-Ecstasy' Test is used for the qualitative detection of MDMA in human urine. This immunoassay is a simplified qualitative screening method that provides only a I his ininutiousses is a varip internaining the need for additional or confirmatory testing, i.e., GC/MS. #### Performance Characteristics: 'RapidOne'-Ecstasy' Test will detect 1000 ng/ml of MDMA in urine. 'RapidOne'-Ecstasy' Test was compared to MedTox Verdict II-Methamphetamine Test. One hundred (100) samples were selected for evaluation. Of the 100 specimens, fifty (50) were found to be drug-free by Syva Emit II. Both immunaoassays correctly identified all the specimens that contained no drug as negative. GC/MS analyses were performed on samples that were screened as positive for the amphetamine group. Specimens containing only MDMA (395 to 19496 ng/ml) were selected for this study. All specimens that contained MDMA concentrations of 1009 ng/ml or greater were found to be positive by both systems. Verdict II did determine three specimens which contained 816, 895 and 958 ng/ml as positive. Reproducibility was evaluated using control urines containing concentrations above and below the stated cut-off. Eighty (80) replicates were run at each concentration, | Concentration<br>(ng/ml) | # | RDS Result | | |--------------------------|----|------------|-----| | | | Pos | Neg | | No drug | 80 | 0 | 80 | | 500 | 80 | 8 | 72 | | 750 | 80 | 40 | 40 | | 1000 | 80 | 78 | 2 | | 1250 | 80 | 80 | 0 | #### Conclusion: 'RapidOne'-Ecstasy' Test is substantially equivalent to MedTox Verdict II-Methamphetamine Test for the qualitative detection of MDMA in human urine. {2}------------------------------------------------ ## Comparison Between 'RapidOne'-Ecstasy Test and MedTox Verdict II-Methamphetamine Test ### 'RapidOne' 'Verdict II' | Intended Use: | For professional use | For professional use | |------------------------|--------------------------|--------------------------| | Type of Assay | Lateral flow immunoassay | Lateral flow immunoassay | | Analyte: | MDMA | MDMA | | Cut-off | 1000 ng/ml | 1000 ng/ml | | Sample<br>Application: | Dipping in specimen | Specimen added dropwise | Assay time: 5-10 minutes 3-8 minutes {3}------------------------------------------------ Image /page/3/Picture/1 description: The image shows the logo for the Department of Health & Human Services - USA. The logo consists of a circle with the text "DEPARTMENT OF HEALTH & HUMAN SERVICES - USA" around the perimeter. Inside the circle is an abstract symbol that resembles a stylized human figure or a bird in flight. The logo is black and white. Food and Drug Administration 2098 Gaither Road Rockville MD 20850 NOV 2 6 2001 Mr. Henry Wells V.P. Product Development American Bio Medica Corporation 9110 Red Branch Road Columbia, MD 21045 k013180 Re: Trade/Device Name: 'RapidOne-Ecstasy' Test Regulation Number: 21 CFR 862.3610 Regulation Name: Methamphetamine test system Regulatory Class: Class II Product Code: DJC Dated: September 21, 2001 Received: September 24, 2001 Dear Mr. Wells: 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 the Code of Federal Regulations, Title 21, Parts 800 to 898. 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 Part 801); good manufacturing practice requirements as set forth in the quality systems (QS) regulation (21 CFR Part 820); and if applicable, the electronic product radiation control provisions (Sections 531-542 of the Act); 21 CFR 1000-1050. {4}------------------------------------------------ #### Page 2 - This letter will allow you to begin marketing your device as described in your 510(k) premarket I his lection. The FDA finding of substantial equivalence of your device to a legally marketed predication. The results in a classification for your device and thus, permits your device to proceed to the market. If you desire specific advice for your device on our labeling regulation (21 CFR Part 801 and 1 11 you dostre by 11 for in vitro diagnostic devices), please contact the Office of Compliance at (301) 594-4588. Additionally, for questions on the promotion and advertising of your device, (301) 59 mto the Office of Compliance at (301) 594-4639. Also, please note the regulation entitled, "Misbranding by reference to premarket notification" (21CFR 807.97). Other general information on your responsibilities under the Act may be obtained 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/cdrb/dsma/dsmamain.html". Sincerely yours, Steven Autman Steven I. Gutman, M.D., M.B.A. Director Division of Clinical Laboratory-Devices Office of Device Evaluation Center for Devices and Radiological Health Enclosure {5}------------------------------------------------ 510(k) Number (if known): _K013180 Device Name:__________________________________________________________________________________________________________________________________________________________________ Indications For Use: 'RapidOne-Ecstasy' Test is a one-step, lateral flow immunoassay for the deection of 3,4-RapidOne-Ecstasy Test Is a one stop, lava a 'Ecstasy') at 1000 ng/ml in urine. 'RapidOne-Ecstasy'-Test is intended for the qualitative detection of MDMA in human urine. 'RapidOne-Ecstasy' Test is intended for professional use. It is not intended for over-the-counter sales to nonprofessionals. The assay is easy to processional use. It is not included withouts result for use immunoassay is a simplified, qualitative screening method that orosides only a preliminary result for use in immunoassay is a smiplified, qualiante screening memoc aller profices and profited and proposition of the matery (GC/MS). 'RapidOue-Ecstasy' Test provides only a preliminary analytical result. A more specific alternate "RapidOne-Ecstasy" Test provides only a premimal y unarythed result. GC/MS is the preferred chemical method. Clinical and professional judgment should be applied to any drug of abuse test result, particularly when preliminary results are use. Sharon pt Rose (Division Sign-Off) Division of Clinical Laboratory Devices KO13180 510(k) Number_ (PLEASE DO NOT WRITE BELOW THIS LINE - CONTINUE ON ANOTHER PAGE IF NEEDED) Concurrence of CDRH, Office of Device Evaluation (ODE) Prescription Use (Per 21 CFR 801.109) ✓ Over-The-Counter Use OR