FDA 510(k)

AQUATULLE FINE MESH NON-ADHERING DRESSING

K-Number: K872759 · 1987-09-04

Decision Date1987-09-04

Product CodeEFQ

DecisionSubstantially Equivalent for Some Indications

Device Summary

AQUATULLE FINE MESH NON-ADHERING DRESSING is the device name listed in this FDA 510(k) record. The listed applicant is Smith & Nephew, Inc.. It received FDA 510(k) clearance on 1987-09-04 under 510(k) number K872759. The device is classified under product code EFQ. FDA Decision: Substantially Equivalent for Some Indications.

Frequently Asked Questions

What is the AQUATULLE FINE MESH NON-ADHERING DRESSING?

AQUATULLE FINE MESH NON-ADHERING DRESSING is a medical device that received FDA 510(k) clearance on 1987-09-04. The listed applicant is Smith & Nephew, Inc.. The 510(k) number is K872759.

When did AQUATULLE FINE MESH NON-ADHERING DRESSING receive FDA 510(k) clearance?

AQUATULLE FINE MESH NON-ADHERING DRESSING received FDA 510(k) clearance on 1987-09-04, under 510(k) number K872759.

Who is the listed applicant for AQUATULLE FINE MESH NON-ADHERING DRESSING?

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

What is the FDA product code for AQUATULLE FINE MESH NON-ADHERING DRESSING?

The FDA product code for AQUATULLE FINE MESH NON-ADHERING DRESSING is EFQ.

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Related Devices (Code: EFQ)

K991757NON-ABSORBABLE GAUZE FOR EXTERNAL USE, STERILE AND NON STERILEFurlong Industries K991215SYMTEX GAUZE PADS (1'S) AND SYMTEX GAUZE SPONGES STERILE 2'S AND STERILE 10'SSymtex Healthcare Corp.K990974VITOP DRESSINGWonder & Bioenergy Hi-Tech America, Inc.K990584GAUZE SPONGES: LAPAROTOMY SPONGE, X-RAY DETECTABLEBroadline Medical Industries K984187CROSSTEX NON-WOVEN SPONGESCrosstex Intl.K983016GAUZE, SPONGES, CAT # 11-003Vitalcare Group, Inc.

Official Source

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