DERMAGRAN HYDROPHILIC WOUND DRESSING— 510(k) K954738

Name: FDA 510(k) clearance K954738
Creator: U.S. Food and Drug Administration
Published: 1995-11-02

Substantially Equivalent

Derma Sciences, Inc.

FDA 510(k) clearance K954738 for DERMAGRAN HYDROPHILIC WOUND DRESSING, Substantially Equivalent on 1995-11-02. Applicant: Derma Sciences, Inc.. Device class: Unclassified.

Clearance details

Applicant: Derma Sciences, Inc.
Product code: Code MGP
Device class: Unclassified
Advisory panel: Unknown
Date received: 1995-10-16
Decision date: 1995-11-02
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Old Forge, PA, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code MGP

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K012997 — COLLATEK FOAM2001-10-25
K001508 — LASERSKIN DRESSING2001-07-25
K990079 — FASTSEAL CHEST WOUND DRESSING1999-12-23
K991214 — SIMPLICARE TRANSPARENT WOUND DRESSING1999-10-14

More clearances from Derma Sciences, Inc.

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K150985 — Medihoney Wound Gel2015-11-19
K133279 — MEDIHONEY WOUND DRESSINGS2015-06-25
K110546 — MEDIHONEY HYDROGEL SHEET DRESSINGS WITH ACTIVE LEPTOSPERMUM HONEY2011-07-27
K101793 — MEDIHONEY GEL DRESSING WITH ACTIVE MANUKA HONEY2011-02-22
K081584 — DERMA SCIENCES OTC MEDIHONEY DRESSINGS WITH ACTIVE MANUKA HONEY2008-06-19

Adverse events under product code MGP

product code MGP

Other: 1
Total: 1

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.