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FDA 510(k)

JAW SPREADER

K-Number: K936050 · 1994-03-24

ApplicantGam Industries, Inc.
Decision Date1994-03-24
Product CodeKBW
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

JAW SPREADER 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 1994-03-24 under 510(k) number K936050. The device is classified under product code KBW. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the JAW SPREADER?

JAW SPREADER is a medical device that received FDA 510(k) clearance on 1994-03-24. The listed applicant is Gam Industries, Inc.. The 510(k) number is K936050.

When did JAW SPREADER receive FDA 510(k) clearance?

JAW SPREADER received FDA 510(k) clearance on 1994-03-24, under 510(k) number K936050.

Who is the listed applicant for JAW SPREADER?

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 JAW SPREADER?

The FDA product code for JAW SPREADER is KBW.

Related Clinical Trials

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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 BREATHERK930401ALUMINUM FOILK926290BURN SHEETK925590MULTI-TRAUMA DRESSING

View all 9 devices →

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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