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FDA 510(k)

DERMAGRAN HYDROPHILIC WOUND DRESSING

K-Number: K954738 · 1995-11-02

ApplicantDerma Sciences, Inc.
Decision Date1995-11-02
Product CodeMGP
DecisionSubstantially Equivalent

Device Summary

DERMAGRAN HYDROPHILIC WOUND DRESSING 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 1995-11-02 under 510(k) number K954738. The device is classified under product code MGP. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DERMAGRAN HYDROPHILIC WOUND DRESSING?

DERMAGRAN HYDROPHILIC WOUND DRESSING is a medical device that received FDA 510(k) clearance on 1995-11-02. The listed applicant is Derma Sciences, Inc.. The 510(k) number is K954738.

When did DERMAGRAN HYDROPHILIC WOUND DRESSING receive FDA 510(k) clearance?

DERMAGRAN HYDROPHILIC WOUND DRESSING received FDA 510(k) clearance on 1995-11-02, under 510(k) number K954738.

Who is the listed applicant for DERMAGRAN HYDROPHILIC WOUND DRESSING?

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 HYDROPHILIC WOUND DRESSING?

The FDA product code for DERMAGRAN HYDROPHILIC WOUND DRESSING is MGP.

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Other records listing Derma Sciences, Inc. as applicant

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.

K110546MEDIHONEY HYDROGEL SHEET DRESSINGS WITH ACTIVE LEPTOSPERMUM HONEYK101793MEDIHONEY GEL DRESSING WITH ACTIVE MANUKA HONEYK081584DERMA SCIENCES OTC MEDIHONEY DRESSINGS WITH ACTIVE MANUKA HONEYK080315DERMA SCIENCES MEDIHONEY DRESSINGS WITH ACTIVE MANUKA HONEYK072956MEDIHONEY PRIMARY DRESSINGS WITH ACTIVE MANUKA HONEYK970660DERMAGRAN WOUND MANAGEMENT SYSTEM

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Related Devices (Code: MGP)

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.

K012995COLLATEK SHEETBiocore Medical Technologies, Inc.K012997COLLATEK FOAMBiocore Medical Technologies, Inc.K001508LASERSKIN DRESSINGFidia Advanced Biopolymers SrlK990079FASTSEAL CHEST WOUND DRESSINGGreenfield Medical Technologies, Inc.K991214SIMPLICARE TRANSPARENT WOUND DRESSINGHollister, Inc.K992302DERMAPHYLYX SKIN PROTECTORS, PROTECT IT SKIN PROTECTORSDermaphylyx, 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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