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FDA 510(k)

DERMAPLEX HYDROGEL WOUND DRESSING

K-Number: K962513 · 1996-09-12

ApplicantMaxxim Medical
Decision Date1996-09-12
Product CodeMGQ
DecisionSubstantially Equivalent for Some Indications

Device Summary

DERMAPLEX HYDROGEL WOUND DRESSING is the device name listed in this FDA 510(k) record. The listed applicant is Maxxim Medical. It received FDA 510(k) clearance on 1996-09-12 under 510(k) number K962513. The device is classified under product code MGQ. FDA Decision: Substantially Equivalent for Some Indications.

Frequently Asked Questions

What is the DERMAPLEX HYDROGEL WOUND DRESSING?

DERMAPLEX HYDROGEL WOUND DRESSING is a medical device that received FDA 510(k) clearance on 1996-09-12. The listed applicant is Maxxim Medical. The 510(k) number is K962513.

When did DERMAPLEX HYDROGEL WOUND DRESSING receive FDA 510(k) clearance?

DERMAPLEX HYDROGEL WOUND DRESSING received FDA 510(k) clearance on 1996-09-12, under 510(k) number K962513.

Who is the listed applicant for DERMAPLEX HYDROGEL WOUND DRESSING?

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

What is the FDA product code for DERMAPLEX HYDROGEL WOUND DRESSING?

The FDA product code for DERMAPLEX HYDROGEL WOUND DRESSING is MGQ.

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Other records listing Maxxim Medical as applicant

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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.

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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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