ALUMINUM FOIL— 510(k) K930401

Name: FDA 510(k) clearance K930401
Creator: U.S. Food and Drug Administration
Published: 1993-05-12

Substantially Equivalent

Gam Industries, Inc.

FDA 510(k) clearance K930401 for ALUMINUM FOIL, Substantially Equivalent on 1993-05-12. Applicant: Gam Industries, Inc.. Device class: Unclassified.

Clearance details

Applicant: Gam Industries, Inc.
Product code: Code MGP
Device class: Unclassified
Advisory panel: Unknown
Date received: 1993-01-26
Decision date: 1993-05-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Petersburg, VA, US

Download summary PDF View on FDA.gov ↗

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K990079 — FASTSEAL CHEST WOUND DRESSING1999-12-23
K991214 — SIMPLICARE TRANSPARENT WOUND DRESSING1999-10-14

More clearances from Gam Industries, Inc.

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K941641 — DISPOSABLE EMERGENCY OBSTETRICAL KIT1994-10-03
K941336 — COMBO MASK1994-09-09
K942021 — MOUTH TO MOUTH BREATHER1994-06-22
K936050 — JAW SPREADER1994-03-24
K926290 — BURN SHEET1993-04-20

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.