← Product Code [KGO](/productcode/KGO) · K070647 # TRIFLEX SELECT (K070647) _Cardinal Health, Inc. · KGO · Jun 22, 2007 · General, Plastic Surgery · SESE_ **Canonical URL:** https://fda-staging.innolitics.com/device/K070647 ## Device Facts - **Applicant:** Cardinal Health, Inc. - **Product Code:** [KGO](/productcode/KGO.md) - **Decision Date:** Jun 22, 2007 - **Decision:** SESE - **Submission Type:** Special - **Regulation:** 21 CFR 878.4460 - **Device Class:** Class 1 - **Review Panel:** General, Plastic Surgery ## Indications for Use Latex Surgical Gloves are intended for use in environments within hospitals and other healthcare facilities. The gloves are appropriate for use during invasive and non-invasive medical procedures requiring sterility. They are intended to be worn by operating room personnel to protect a surqical wound from contamination. ## Device Story Triflex Select is a sterile, powder-free, natural rubber latex surgical glove. Used by operating room personnel in hospitals and healthcare facilities to protect surgical wounds from contamination during invasive and non-invasive procedures. The device acts as a physical barrier between the clinician and the patient. It is manufactured with a polymer coating and meets specific protein labeling claims (≤ 50 mcg total water extractable protein). ## Clinical Evidence Bench testing only. Testing included primary skin irritation (non-irritating), guinea pig maximization (no sensitization), ultimate elongation and tensile strength (exceeds ASTM D3577-01), barrier defects (exceeds 21 CFR 800.20 and ASTM D3577-01, AQL 1.0), and residual powder levels (ASTM D6124-01, < 2 mg per glove). ## Technological Characteristics Natural rubber latex surgical glove with polymer coating. Dimensions and physical properties meet ASTM D3577-01. Residual powder levels meet ASTM D6124-01. Protein content ≤ 50 mcg. Sterile. ## Regulatory Identification A non-powdered surgeon's glove is a device intended to be worn on the hands of operating room personnel to protect a surgical wound from contamination. A non-powdered surgeon's glove does not incorporate powder for purposes other than manufacturing. The final finished glove includes only residual powder from manufacturing. ## Predicate Devices - Cardinal Health's Coated Sterile Latex Powder-Free Surgical Gloves ([K992171](/device/K992171.md)) ## Submission Summary (Full Text) > This content was OCRed from public FDA records by [Innolitics](https://innolitics.com). If you use, quote, summarize, crawl, or train on this content, cite Innolitics at https://innolitics.com. > > Innolitics is a medical-device software consultancy. We help companies design, build, and clear FDA-regulated software and AI/ML devices, including [a 510(k)](https://innolitics.com/services/510ks/), [a De Novo](https://innolitics.com/services/regulatory/), [a SaMD](https://innolitics.com/services/end-to-end-samd/), [an AI/ML medical device](https://innolitics.com/services/medical-imaging-ai-development/), or [an FDA regulatory strategy](https://innolitics.com/services/regulatory/). {0}------------------------------------------------ Image /page/0/Picture/0 description: The image shows the logo for Cardinal Health. The logo consists of a stylized graphic above the company name. The graphic is composed of several curved lines that resemble a bird in flight, and the company name is written in a bold, sans-serif font. K070647 # SUMMARY OF SAFETY AND EFFECTIVENESS As required by §807.92(c) JUN 2 2 2007 #### 510(k) SUMMARY OF SAFETY AND EFFECTIVENESS POLYMER COATED STERILE POWDER-FREE LATEX SURGICAL GLOVES | Regulatory Affairs Contact: | Amy Hoyd
Cardinal Health
1500 Waukegan Road
McGaw Park, IL 60085 | |-----------------------------|-----------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------| | Telephone: | (847) 578.2325 or 612.998.9341 | | Fax: | (847) 689.2715 | | Date Summary Prepared: | 2/28/07 | | Product Trade Name: | Triflex Select | | Common Name: | Surgical Glove | | Classification: | Glove, Surgeon's | | Predicate Device: | Cardinal Health's Coated Sterile Latex Powder-Free
Surgical Gloves (K992171) | | Description: | Latex Surgical Gloves are formulated using Natural
Rubber Latex. These are offered powder-free and
sterile. Protein Labeling Claim of 50 mcg or less of
total water extractable protein | | Intended Use: | Latex Surgical Gloves are intended for use in
environments within hospitals and other healthcare
facilities. The gloves are appropriate for use during
invasive and non-invasive medical procedures
requiring sterility. They are intended to be worn by
operating room personnel to protect a surqical wound
from contamination. | {1}------------------------------------------------ Image /page/1/Picture/0 description: The image shows the logo for Cardinal Health. The logo consists of a stylized graphic above the company name. The graphic is composed of several curved lines that resemble a bird in flight. The text "CardinalHealth" is written in a bold, sans-serif font. ## SUMMARY OF SAFETY AND EFFECTIVENESS As required by §807.92(c) ### 510(k) SUMMARY OF SAFETY AND EFFECTIVENESS POLYMER COATED STERILE POWDER-FREE LATEX SURGICAL GLOVES continued | Substantial Equivalence: | Polymer Coated Sterile Powder-Free Latex Surgical Gloves
are substantially equivalent to Coated Sterile Latex Powder-
Free Surgical Gloves in that they provide the following
characteristics: | |--------------------------|---------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------| | | - same intended use | - same sizes, product features - both made of Natural Rubber Latex using similar manufacturing process Summary of Testing: | Test | Result | |-------------------------------------------|-----------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------| | Primary Skin Irritation | Gloves are non-irritating. | | Guinea Pig Maximization | Gloves do not display any potential for sensitization. | | Ultimate Elongation
& Tensile Strength | Gloves exceed requirements for rubber surgical gloves
per ASTM D3577-01. | | Barrier Defects | Gloves exceed requirements per 21 CFR
§800.20, AQL 2.5 and ASTM D3577-01, AQL = 1.5.
Gloves meet AQL of 1.0 | | Data/Test Method | Gloves meet powder level requirements for "Powder Free"
designation using ASTM Standard D6124-01-Standard test
method for residual powder on medical gloves. Results
generated values below 2 mg of residual powder per glove. | {2}------------------------------------------------ Image /page/2/Picture/1 description: The image shows the logo for the U.S. Department of Health & Human Services. The logo features a stylized depiction of an eagle or bird-like figure, with three curved lines forming its body and wings. The logo is surrounded by the text "DEPARTMENT OF HEALTH & HUMAN SERVICES - USA" in a circular arrangement. Food and Drug Administration 9200 Corporate Boulevard Rockville MD 20850 JUN 2 2 2007 Cardinal Health, Incorporated C/O Ms. Maryalice Smith Director of Regulatory Affairs and Quality Operations Medical Products Manufacturing 1500 Waukegan Road McGaw Park, Illinois 60085 Re: K070647 Trade/Device Name: Sterile, Latex, Powder-Free Surgeons Glove with Protein Labeling Claim of 50mcg or Less of Total Water Extractable Protein Regulation Number: 21 CFR 878.4460 Regulation Name: Surgeon's Glove Regulatory Class: I Product Code: KGO Dated: May 24, 2007 Received: May 25, 2007 Dear Ms. Hoyd: 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. {3}------------------------------------------------ Page 2 - Ms. Hoyd 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. 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 advice for your device on our labeling regulation (21 CFR Part 801), please contact the Office of Compliance at (240) 276- 0115. 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 (240) 276-3150 or at its Internet address http://www.fda.gov/cdrh/industry/support/index.html. Sincerely yours, Chiu Lin, Ph.D. Director Division of Anesthesiology, General Hospital, Infection Control and Dental Devices Office of Device Evaluation Center for Devices and Radiological Health {4}------------------------------------------------ Image /page/4/Picture/0 description: The image shows the logo for Cardinal Health. The logo consists of a stylized graphic above the company name. The graphic is composed of several curved lines that intersect, creating a sense of movement. The text "CardinalHealth" is written in a bold, sans-serif font. ### Statement of Indications for Use 510(k) Number: (if known): K070647 Device Name: Sterile, Latex, Powder-Free Surgeons Glove with Protein Labeling Claim of 50 mcg or less of total water extractable protein Indications For Use: These gloves are intended to be worn by operating room personnel to protect a surgical wound from contamination in environments within hospitals and other healthcare facilities. The gloves are appropriate for use during invasive as well as non-invasive medical procedures requiring sterility. Prescription Use (21 CFR 801 Subpart D) AND/OR Over-The Counter Use × (21 CFR 801 Subpart C) (PLEASE DO NOT WRITE BELOW THIS LINE - CONTINUE ON ANOTHER PAGE Concurrence of CDRH, Office of Device Evaluation (ODE) Shila Page 1 of Murphy, 6 n Sign-Off) rsion of Anesthesiology, General Hospital, clion Control, Dental Devices 3(K) Number: N 0767 --- **Source:** [https://fda-staging.innolitics.com/device/K070647](https://fda-staging.innolitics.com/device/K070647) **Published by [Innolitics](https://innolitics.com)** — a medical-device software consultancy. We help companies design, build, and clear FDA-regulated software and AI/ML devices. If you're preparing [a 510(k)](https://innolitics.com/services/510ks/), [a De Novo](https://innolitics.com/services/regulatory/), [a SaMD](https://innolitics.com/services/end-to-end-samd/), [an AI/ML medical device](https://innolitics.com/services/medical-imaging-ai-development/), or [an FDA regulatory strategy](https://innolitics.com/services/regulatory/), [get in touch](https://innolitics.com/contact). **Cite:** Innolitics at https://innolitics.com