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FDA 510(k)

CATHETERIZATION FORCEP

K-Number: K792494 · 1979-12-20

ApplicantC. Intl.
Decision Date1979-12-20
Product CodeGEN
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

CATHETERIZATION FORCEP is the device name listed in this FDA 510(k) record. The listed applicant is C. Intl.. It received FDA 510(k) clearance on 1979-12-20 under 510(k) number K792494. 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 CATHETERIZATION FORCEP?

CATHETERIZATION FORCEP is a medical device that received FDA 510(k) clearance on 1979-12-20. The listed applicant is C. Intl.. The 510(k) number is K792494.

When did CATHETERIZATION FORCEP receive FDA 510(k) clearance?

CATHETERIZATION FORCEP received FDA 510(k) clearance on 1979-12-20, under 510(k) number K792494.

Who is the listed applicant for CATHETERIZATION FORCEP?

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

What is the FDA product code for CATHETERIZATION FORCEP?

The FDA product code for CATHETERIZATION FORCEP is GEN.

Related Clinical Trials

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.

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Other records listing C. Intl. 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.

K790855SURGICAL DRAPE CLIP #201K790853EASY-SPECK790852VAGI-SPECK790851VAGI-PRESS #401K790854FORCEPS #101 AND #102K790856PROCTOSCOPE #501

View all 7 devices →

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

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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