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FDA 510(k)

FORCEP, THUMB

K-Number: K760507 · 1976-11-12

ApplicantAcme United Corp.
Decision Date1976-11-12
Product CodeGEN
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

FORCEP, THUMB is the device name listed in this FDA 510(k) record. The listed applicant is Acme United Corp.. It received FDA 510(k) clearance on 1976-11-12 under 510(k) number K760507. The device is classified under product code GEN. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FORCEP, THUMB?

FORCEP, THUMB is a medical device that received FDA 510(k) clearance on 1976-11-12. The listed applicant is Acme United Corp.. The 510(k) number is K760507.

When did FORCEP, THUMB receive FDA 510(k) clearance?

FORCEP, THUMB received FDA 510(k) clearance on 1976-11-12, under 510(k) number K760507.

Who is the listed applicant for FORCEP, THUMB?

The FDA 510(k) record lists Acme United Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for FORCEP, THUMB?

The FDA product code for FORCEP, THUMB is GEN.

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Other records listing Acme United Corp. as applicant

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Related Devices (Code: GEN)

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.

K031828NATURALASE LP ND:YAG LASERFocus Medical, LLCK953962FORCEPSBiopsys Medical, Inc.K932385SUTURE REMOVING FORCEPSRocket of London, Ltd.K904723FORCEPSMinto Research & Development, Inc.K911159PALPATION PROBENorthgate Technologies, Inc.K900951GS-7000 CLIP-APPLYING FORCEP, 10MM, MEDIUM CLIPSolos Endoscopy, 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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