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FDA 510(k)

DERMAGRAN WOUND CLEANSER WITH ZINC

K-Number: K945802 · 1995-02-27

ApplicantDerma Sciences, Inc.
Decision Date1995-02-27
Product CodeKMF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

DERMAGRAN WOUND CLEANSER WITH ZINC is the device name listed in this FDA 510(k) record. The listed applicant is Derma Sciences, Inc.. It received FDA 510(k) clearance on 1995-02-27 under 510(k) number K945802. 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 DERMAGRAN WOUND CLEANSER WITH ZINC?

DERMAGRAN WOUND CLEANSER WITH ZINC is a medical device that received FDA 510(k) clearance on 1995-02-27. The listed applicant is Derma Sciences, Inc.. The 510(k) number is K945802.

When did DERMAGRAN WOUND CLEANSER WITH ZINC receive FDA 510(k) clearance?

DERMAGRAN WOUND CLEANSER WITH ZINC received FDA 510(k) clearance on 1995-02-27, under 510(k) number K945802.

Who is the listed applicant for DERMAGRAN WOUND CLEANSER WITH ZINC?

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

What is the FDA product code for DERMAGRAN WOUND CLEANSER WITH ZINC?

The FDA product code for DERMAGRAN WOUND CLEANSER WITH ZINC is KMF.

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Other records listing Derma Sciences, 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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