FDA 510(k)

ALLEVYN DRESSING (LABELING REVISED)

K-Number: K901877 · 1990-06-22

Decision Date1990-06-22

Product CodeKMF

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

ALLEVYN DRESSING (LABELING REVISED) is the device name listed in this FDA 510(k) record. The listed applicant is Smith & Nephew United, Inc.. It received FDA 510(k) clearance on 1990-06-22 under 510(k) number K901877. The device is classified under product code KMF. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ALLEVYN DRESSING (LABELING REVISED)?

ALLEVYN DRESSING (LABELING REVISED) is a medical device that received FDA 510(k) clearance on 1990-06-22. The listed applicant is Smith & Nephew United, Inc.. The 510(k) number is K901877.

When did ALLEVYN DRESSING (LABELING REVISED) receive FDA 510(k) clearance?

ALLEVYN DRESSING (LABELING REVISED) received FDA 510(k) clearance on 1990-06-22, under 510(k) number K901877.

Who is the listed applicant for ALLEVYN DRESSING (LABELING REVISED)?

The FDA 510(k) record lists Smith & Nephew United, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ALLEVYN DRESSING (LABELING REVISED)?

The FDA product code for ALLEVYN DRESSING (LABELING REVISED) is KMF.

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Other records listing Smith & Nephew United, Inc. as applicant

K963096ALLEVYN HYDRO POLY DRESSING ND ALL TRAC DRESSING K961775PROFORE FOUR-LAYER BANDAGE SYSTEM KIT K945330ALLEVYN ADHESIVE K943619CAVI-CARE CONFORMING FOAM DRESSING K942748INTRASITE K935705ALLEVYN ISLAND WOUND DRESSING

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Related Devices (Code: KMF)

K241916TearRepair Liquid Skin ProtectantOptmed, Inc.K182733Rochal Bioshield Silicone FilmRochal Industries, LLC K171148Aleo BME Liquid BandageAleo Bme, Inc.K153571Cavilon Advanced High Endurance Skin Protectant3M Healthcare K160684Atteris No-Sting Skin ProtectantRochal Industries, LLC K120059LIQUID BANDAGEChesson Laboratory Associates, Inc.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.