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FDA 510(k)

ALUMINUM FOIL

K-Number: K930401 · 1993-05-12

ApplicantGam Industries, Inc.
Decision Date1993-05-12
Product CodeMGP
DecisionSubstantially Equivalent

Device Summary

ALUMINUM FOIL is the device name listed in this FDA 510(k) record. The listed applicant is Gam Industries, Inc.. It received FDA 510(k) clearance on 1993-05-12 under 510(k) number K930401. The device is classified under product code MGP. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ALUMINUM FOIL?

ALUMINUM FOIL is a medical device that received FDA 510(k) clearance on 1993-05-12. The listed applicant is Gam Industries, Inc.. The 510(k) number is K930401.

When did ALUMINUM FOIL receive FDA 510(k) clearance?

ALUMINUM FOIL received FDA 510(k) clearance on 1993-05-12, under 510(k) number K930401.

Who is the listed applicant for ALUMINUM FOIL?

The FDA 510(k) record lists Gam Industries, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ALUMINUM FOIL?

The FDA product code for ALUMINUM FOIL is MGP.

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Other records listing Gam Industries, 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.

K941641DISPOSABLE EMERGENCY OBSTETRICAL KITK941336COMBO MASKK942021MOUTH TO MOUTH BREATHERK936050JAW SPREADERK926290BURN SHEETK925590MULTI-TRAUMA DRESSING

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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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