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FDA 510(k)

DEROYAL WOUND CARE MULTIDEX GEL WOUND DRESSING

K-Number: K952775 · 1995-10-06

ApplicantDeroyal Industries, Inc.
Decision Date1995-10-06
Product CodeMGQ
DecisionSubstantially Equivalent for Some Indications

Device Summary

DEROYAL WOUND CARE MULTIDEX GEL WOUND DRESSING is the device name listed in this FDA 510(k) record. The listed applicant is Deroyal Industries, Inc.. It received FDA 510(k) clearance on 1995-10-06 under 510(k) number K952775. The device is classified under product code MGQ. FDA Decision: Substantially Equivalent for Some Indications.

Frequently Asked Questions

What is the DEROYAL WOUND CARE MULTIDEX GEL WOUND DRESSING?

DEROYAL WOUND CARE MULTIDEX GEL WOUND DRESSING is a medical device that received FDA 510(k) clearance on 1995-10-06. The listed applicant is Deroyal Industries, Inc.. The 510(k) number is K952775.

When did DEROYAL WOUND CARE MULTIDEX GEL WOUND DRESSING receive FDA 510(k) clearance?

DEROYAL WOUND CARE MULTIDEX GEL WOUND DRESSING received FDA 510(k) clearance on 1995-10-06, under 510(k) number K952775.

Who is the listed applicant for DEROYAL WOUND CARE MULTIDEX GEL WOUND DRESSING?

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

What is the FDA product code for DEROYAL WOUND CARE MULTIDEX GEL WOUND DRESSING?

The FDA product code for DEROYAL WOUND CARE MULTIDEX GEL WOUND DRESSING is MGQ.

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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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