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FDA 510(k)

MULTI-TRAUMA DRESSING

K-Number: K925590 · 1993-04-08

ApplicantGam Industries, Inc.
Decision Date1993-04-08
Product CodeNAB
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

MULTI-TRAUMA DRESSING 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 1993-04-08 under 510(k) number K925590. The device is classified under product code NAB. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MULTI-TRAUMA DRESSING?

MULTI-TRAUMA DRESSING is a medical device that received FDA 510(k) clearance on 1993-04-08. The listed applicant is Gam Industries, Inc.. The 510(k) number is K925590.

When did MULTI-TRAUMA DRESSING receive FDA 510(k) clearance?

MULTI-TRAUMA DRESSING received FDA 510(k) clearance on 1993-04-08, under 510(k) number K925590.

Who is the listed applicant for MULTI-TRAUMA DRESSING?

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 MULTI-TRAUMA DRESSING?

The FDA product code for MULTI-TRAUMA DRESSING is NAB.

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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 SPREADERK930401ALUMINUM FOILK926290BURN SHEET

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Related Devices (Code: NAB)

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.

K946015IVALON EXTERNAL SPONGEIvalonK940755ISOLYER (4X4, 8PLY)Isolyer Co.K931610OMNISORB II, NONWOVEN SPONGE, STERILE AND NONOmni Mfg., Inc.K926072K-BAND AND K-CREPEParema , Ltd.K915591STERILE GAUZE PADSEagle Medical, Inc.K924650GAUZE SPONGESDav-Mar Medical Products, 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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