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FDA 510(k)

ABSORBENT GAUZE ROLL

K-Number: K890672 · 1989-04-07

ApplicantSmith & Nephew United, Inc.
Decision Date1989-04-07
Product CodeNAB
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ABSORBENT GAUZE ROLL 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 1989-04-07 under 510(k) number K890672. The device is classified under product code NAB. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ABSORBENT GAUZE ROLL?

ABSORBENT GAUZE ROLL is a medical device that received FDA 510(k) clearance on 1989-04-07. The listed applicant is Smith & Nephew United, Inc.. The 510(k) number is K890672.

When did ABSORBENT GAUZE ROLL receive FDA 510(k) clearance?

ABSORBENT GAUZE ROLL received FDA 510(k) clearance on 1989-04-07, under 510(k) number K890672.

Who is the listed applicant for ABSORBENT GAUZE ROLL?

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 ABSORBENT GAUZE ROLL?

The FDA product code for ABSORBENT GAUZE ROLL is NAB.

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

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Related Devices (Code: NAB)

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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.

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