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FDA 510(k)

ACTICOAT SILVER COATED DRESSING

K-Number: K955453 · 1996-05-31

ApplicantWestaim Technologies, Inc.
Decision Date1996-05-31
Product CodeKMF
Advisory CommitteeHO
DecisionSubstantially Equivalent for Some Indications

Device Summary

ACTICOAT SILVER COATED DRESSING is the device name listed in this FDA 510(k) record. The listed applicant is Westaim Technologies, Inc.. It received FDA 510(k) clearance on 1996-05-31 under 510(k) number K955453. The device is classified under product code KMF. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent for Some Indications.

Frequently Asked Questions

What is the ACTICOAT SILVER COATED DRESSING?

ACTICOAT SILVER COATED DRESSING is a medical device that received FDA 510(k) clearance on 1996-05-31. The listed applicant is Westaim Technologies, Inc.. The 510(k) number is K955453.

When did ACTICOAT SILVER COATED DRESSING receive FDA 510(k) clearance?

ACTICOAT SILVER COATED DRESSING received FDA 510(k) clearance on 1996-05-31, under 510(k) number K955453.

Who is the listed applicant for ACTICOAT SILVER COATED DRESSING?

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

What is the FDA product code for ACTICOAT SILVER COATED DRESSING?

The FDA product code for ACTICOAT SILVER COATED DRESSING is KMF.

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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.

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