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FDA 510(k)

NASAL CAVITY WOUND DRESSING

K-Number: K923957 · 1993-05-05

ApplicantSmith & Nephew Richards, Inc.
Decision Date1993-05-05
Product CodeKMF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

NASAL CAVITY WOUND DRESSING is the device name listed in this FDA 510(k) record. The listed applicant is Smith & Nephew Richards, Inc.. It received FDA 510(k) clearance on 1993-05-05 under 510(k) number K923957. 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 NASAL CAVITY WOUND DRESSING?

NASAL CAVITY WOUND DRESSING is a medical device that received FDA 510(k) clearance on 1993-05-05. The listed applicant is Smith & Nephew Richards, Inc.. The 510(k) number is K923957.

When did NASAL CAVITY WOUND DRESSING receive FDA 510(k) clearance?

NASAL CAVITY WOUND DRESSING received FDA 510(k) clearance on 1993-05-05, under 510(k) number K923957.

Who is the listed applicant for NASAL CAVITY WOUND DRESSING?

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

What is the FDA product code for NASAL CAVITY WOUND DRESSING?

The FDA product code for NASAL CAVITY WOUND DRESSING is KMF.

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

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Related Devices (Code: KMF)

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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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