MICRO-COLL COLLAGEN DERMAL WOUND SPRAY— 510(k) K920642

Name: FDA 510(k) clearance K920642
Creator: U.S. Food and Drug Administration
Published: 1992-04-29

Substantially Equivalent

Micro-Collagen Pharmaceutics, Ltd.

FDA 510(k) clearance K920642 for MICRO-COLL COLLAGEN DERMAL WOUND SPRAY, Substantially Equivalent on 1992-04-29. Applicant: Micro-Collagen Pharmaceutics, Ltd.. Device class: Unclassified.

Clearance details

Applicant: Micro-Collagen Pharmaceutics, Ltd.
Product code: Code MGQ
Device class: Unclassified
Advisory panel: Unknown
Date received: 1992-02-12
Decision date: 1992-04-29
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Bangor, PA, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code MGQ

view all

K171879 — HylaGuard Moisturizing Cream2017-10-16
K083024 — HYLATOPIC EMOLLIENT FOAM2009-03-27
K041342 — IMPRUV A.I. CREAM WOUND AND SKIN EMULSION2005-07-19
K041268 — SILVERSITE OR CALGITROL2004-09-20
K040019 — SILVERSEAL2004-07-23

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.