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FDA 510(k)

ACRYDERM GEL WOUND DRESSING

K-Number: K970693 · 1997-03-21

ApplicantAcrymed, Inc.
Decision Date1997-03-21
Product CodeMGQ
DecisionSubstantially Equivalent for Some Indications

Device Summary

ACRYDERM GEL WOUND DRESSING is the device name listed in this FDA 510(k) record. The listed applicant is Acrymed, Inc.. It received FDA 510(k) clearance on 1997-03-21 under 510(k) number K970693. The device is classified under product code MGQ. FDA Decision: Substantially Equivalent for Some Indications.

Frequently Asked Questions

What is the ACRYDERM GEL WOUND DRESSING?

ACRYDERM GEL WOUND DRESSING is a medical device that received FDA 510(k) clearance on 1997-03-21. The listed applicant is Acrymed, Inc.. The 510(k) number is K970693.

When did ACRYDERM GEL WOUND DRESSING receive FDA 510(k) clearance?

ACRYDERM GEL WOUND DRESSING received FDA 510(k) clearance on 1997-03-21, under 510(k) number K970693.

Who is the listed applicant for ACRYDERM GEL WOUND DRESSING?

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 GEL WOUND DRESSING?

The FDA product code for ACRYDERM GEL WOUND DRESSING is MGQ.

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Other records listing Acrymed, Inc. as applicant

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K091354ACRYDERM SILVER ANTIMICROBIAL FOAM WOUND DRESSINGK083103ACRYDERM ANTIMICROBIAL SILVER GEL WOUND DRESSING MODEL #BK082459ACRYDERM ABSORBENT OXYGEN DRESSINGK070333ACRYDERM SILVER ANTIMICROBIAL OTC WOUND GELK061232ACRYDERM SILVER ANTIMICROBIAL THIN FILM, MODEL 2006K011994ACRYDERM SILVER ANTTIMICROBIAL WOUND GEL MODEL# A-002101

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Related Devices (Code: MGQ)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K171879HylaGuard Moisturizing CreamFounders Science Group, LLCK083024HYLATOPIC EMOLLIENT FOAMCollegium Pharmaceutical IncorporatedK041342IMPRUV A.I. CREAM WOUND AND SKIN EMULSIONStiefel Laboratories, Inc.K041268SILVERSITE OR CALGITROLAdriK040019SILVERSEALNoble Fiber TechnologiesK040517TENDERWET ACTIVEMedline Industries, Inc.

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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