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FDA 510(k)

ACRYDERM SILVER ANTTIMICROBIAL WOUND GEL MODEL# A-002101

K-Number: K011994 · 2001-11-08

ApplicantAcrymed, Inc.
Decision Date2001-11-08
Product CodeMGQ
DecisionSubstantially Equivalent

Device Summary

ACRYDERM SILVER ANTTIMICROBIAL WOUND GEL MODEL# A-002101 is the device name listed in this FDA 510(k) record. The listed applicant is Acrymed, Inc.. It received FDA 510(k) clearance on 2001-11-08 under 510(k) number K011994. The device is classified under product code MGQ. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ACRYDERM SILVER ANTTIMICROBIAL WOUND GEL MODEL# A-002101?

ACRYDERM SILVER ANTTIMICROBIAL WOUND GEL MODEL# A-002101 is a medical device that received FDA 510(k) clearance on 2001-11-08. The listed applicant is Acrymed, Inc.. The 510(k) number is K011994.

When did ACRYDERM SILVER ANTTIMICROBIAL WOUND GEL MODEL# A-002101 receive FDA 510(k) clearance?

ACRYDERM SILVER ANTTIMICROBIAL WOUND GEL MODEL# A-002101 received FDA 510(k) clearance on 2001-11-08, under 510(k) number K011994.

Who is the listed applicant for ACRYDERM SILVER ANTTIMICROBIAL WOUND GEL MODEL# A-002101?

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

What is the FDA product code for ACRYDERM SILVER ANTTIMICROBIAL WOUND GEL MODEL# A-002101?

The FDA product code for ACRYDERM SILVER ANTTIMICROBIAL WOUND GEL MODEL# A-002101 is MGQ.

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Related Devices (Code: MGQ)

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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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