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FDA 510(k)

STRAITH CHISEL FORCEPS

K-Number: K801075 · 1980-05-20

ApplicantSurgical Technology Laboratories, Inc.
Decision Date1980-05-20
Product CodeGEN
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

STRAITH CHISEL FORCEPS is the device name listed in this FDA 510(k) record. The listed applicant is Surgical Technology Laboratories, Inc.. It received FDA 510(k) clearance on 1980-05-20 under 510(k) number K801075. 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 STRAITH CHISEL FORCEPS?

STRAITH CHISEL FORCEPS is a medical device that received FDA 510(k) clearance on 1980-05-20. The listed applicant is Surgical Technology Laboratories, Inc.. The 510(k) number is K801075.

When did STRAITH CHISEL FORCEPS receive FDA 510(k) clearance?

STRAITH CHISEL FORCEPS received FDA 510(k) clearance on 1980-05-20, under 510(k) number K801075.

Who is the listed applicant for STRAITH CHISEL FORCEPS?

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

What is the FDA product code for STRAITH CHISEL FORCEPS?

The FDA product code for STRAITH CHISEL FORCEPS is GEN.

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Other records listing Surgical Technology Laboratories, 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.

K170582Saf-T-Vac Smoke and Fluid EvacuatorK021889SURGIFORM AUGMENTATION MATERIAL (S.F.A.M.)K983756SURGIFORM ANATOMICAL MALARK983755NASAL DORSAL SERIESK983754STANDARD CHINK964443SURGIFORM ANATOMICAL MALAR

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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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