CONVERTORS, SPUNBONDED, FLASHSPUN POLYOLEFIN GOWNS

{0}------------------------------------------------ AUG 2 4 1998 **Allegiance** Park, Illinois 60085-678 K982369 ## SMDA REQUIREMENTS (continued) XII. # 510(k) SUMMARY OF SAFETY AND EFFECTIVENESS Convertors® Spunbonded, Flashspun Polyolefin Gowns Intended Use: Substantial Equivalence: patient and the operating room personnel from the transfer of microorganisms, body fluids and particulate material. The Convertors® Spunbonded, Flashspun surgical procedures to protect both the surgical Surgical apparel are devices intended to be worn by operating room personnel during Polyolefin gowns are substantially equivalent to the Convertors® Optima standard, fabric- and poly-reinforced gowns in that: - the intended use is the same - the performance attributes are the similar All materials used in the fabrication of this Convertors® Spunbonded, Flashspun Polyolefin evaluated through biological aowns were qualification safety tests as outlined in ISO 10993 Part-1 "Biological Evaluation of Medical Devices". The biocompatibility tests performed were sensitization, cvtotoxicity, and irritation/ intracutaneous reactivity. These materials also were tested in accordance with industry recognized test methods and were found to be acceptable for the intended use. Summary of testing: {1}------------------------------------------------ #### XIII. SAMPLE A drawing of the standard, fabric- and poly-reinforced gowns are enclosed to visually assist with the review. (See Appendix D). #### XIV. KIT INFORMATION Each gown is packaged with a towel. The towel is the same towel that is currently placed in our gown packs. This towel has been used safely and effectively for many years as a component of the gown This premarket notification (510(k)) is to introduce standard, pack. fabric and poly-reinforced gowns constructed of Spunbonded, Flashspun Polyolefin fabric. There is no change to the towel contained within this pack. ### XV. 21 CFR 807.95 -CONFIDENTIALITY Allegiance Healthcare Corporation regards its intent to market the Convertors® Spunbonded, Flashspun Polyolefin gown as confidential commercial information. Allegiance Healthcare Corporation has not divulged this intent to market information to anyone other than Allegiance employees and even then on a need-to-know basis. Therefore, we request that FDA treat this information in a confidential manner. {2}------------------------------------------------ Image /page/2/Picture/1 description: The image shows the seal of the Department of Health & Human Services - USA. The seal is circular and contains the text "DEPARTMENT OF HEALTH & HUMAN SERVICES - USA" around the perimeter. In the center of the seal is an abstract design of a human figure with three arms. Food and Drug Administration 9200 Corporate Boulevard Rockville MD 20850 AUG 2 4 1998 Ms. Sharon Robbins Requlatory Affairs Manager Allegiance Healthcare Corporation 1500 Waukegan Road MPWM McGaw Park, Illinois 60085-6787 Re : K982369 Convertors® Spunbonded, Flashspun Trade Name: Polyolefin Gowns, Sterile Regulatory Class: II Product Code: FYC Dated: July 1, 1998 Received: July 7, 1998 Dear Ms. Robbins: We have reviewed your Section 510(k) notification of intent to market the device referenced above and we 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). You may, therefore, market the device, subject to the general controls provisions of the Act. The general controls provisions of the Act include reguirements 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 (Premarket Approval), it may be subject to such additional controls. Existing major requlations affecting your device can be found in the Code of Federal Requlations, Title 21, Parts 800 to 895. ਰ substantially equivalent determination assumes compliance with the Current Good Manufacturing Practice requirements, as set forth in the Quality System Regulation (QS) for Medical General regulation (21 CFR Part 820) and that, Devices: through periodic QS inspections, the Food and Drug Administration (FDA) will verify such assumptions. Failure to comply with the GMP regulation may result in regulatory In addition, FDA may publish further announcements action. concerning your device in the Federal Reqister. Please note: this response to your premarket notification submission does not affect any obligation you might have under sections 531 {3}------------------------------------------------ Page 2 - Ms. Robbins through 542 of the Act for devices under the Electronic Product Radiation Control provisions, or other Federal laws or requlations. This letter will allow you to begin marketing your device as described in your 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 and additionally 809.10 for in vitro diagnostic devices), please contact the Office of Compliance at (301) 594-4692. Additionally, for questions on the promotion and advertising of your device, please contact 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 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, S. Butman for Timothy A. Ulatowski Director Division of Dental, Infection Control, and General Hospital Devices Office of Device Evaluation Center for Devices and Radiological Health Enclosure ... ...... {4}------------------------------------------------ **Allegiance** Allegiance Healthcare Corporation 1500 Waukegan Road McGaw Park, Illinois 60085-6787 7.473.1500 AX: 847.785.2461 Page 1 of 1 510(k) Number (if known): K982369 Device Name: Convertors® Spunbonded, Flashspun Polyolefin Gowns, Sterile Indications For Use: The Convertors® Spunbonded, Flashspun Polyolefin Gowns are devices intended to be worn by operating room personnel during surgical procedures to protect both the surgical patient and the operating room personnel from the transfer of microorganisms, body fluids and particulate material. (PLEASE DO NOT WRITE BELOW THIS LINE - CONTINUE ON ANOTHER PAGE) Concurrence of CDRH, Office of Device Evaluation (ODE) Prescription Use (Per 21 CFR 801.109) or Over-The Counter Use Chim S. f. (Division Sign-Off) Division of Dental, Infection Control, and General Hospital Device 510(k) Number