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FDA 510(k)

O'CONNOR HOOK PUNCH FORCEP

K-Number: K813245 · 1981-12-29

ApplicantShutt Instruments
Decision Date1981-12-29
Product CodeGEN
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

O'CONNOR HOOK PUNCH FORCEP is the device name listed in this FDA 510(k) record. The listed applicant is Shutt Instruments. It received FDA 510(k) clearance on 1981-12-29 under 510(k) number K813245. 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 O'CONNOR HOOK PUNCH FORCEP?

O'CONNOR HOOK PUNCH FORCEP is a medical device that received FDA 510(k) clearance on 1981-12-29. The listed applicant is Shutt Instruments. The 510(k) number is K813245.

When did O'CONNOR HOOK PUNCH FORCEP receive FDA 510(k) clearance?

O'CONNOR HOOK PUNCH FORCEP received FDA 510(k) clearance on 1981-12-29, under 510(k) number K813245.

Who is the listed applicant for O'CONNOR HOOK PUNCH FORCEP?

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

What is the FDA product code for O'CONNOR HOOK PUNCH FORCEP?

The FDA product code for O'CONNOR HOOK PUNCH FORCEP is GEN.

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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.K900952GS-1200 GRASPING/EXTRACTING FORCEP, 10MMSolos Endoscopy, Inc.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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