DERMAGRAN (ZINC SALINE) HYDROGEL WOUND DRESSING— 510(k) K954664

Name: FDA 510(k) clearance K954664
Creator: U.S. Food and Drug Administration
Published: 1995-11-01

Substantially Equivalent for Some Indications

Derma Sciences, Inc.

FDA 510(k) clearance K954664 for DERMAGRAN (ZINC SALINE) HYDROGEL WOUND DRESSING, Substantially Equivalent for Some Indications on 1995-11-01. Applicant: Derma Sciences, Inc.. Device class: Unclassified.

Clearance details

Applicant: Derma Sciences, Inc.
Product code: Code MGQ
Device class: Unclassified
Advisory panel: Unknown
Date received: 1995-10-10
Decision date: 1995-11-01
Decision: Substantially Equivalent for Some Indications
Clearance type: Traditional
Location: Old Forge, PA, US

Download summary PDF View on FDA.gov ↗

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Adverse events under product code MGQ

product code MGQ

Death: 16
Total: 16

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.