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FDA 510(k)

VASCULAR FORCEPS & CLAMPS

K-Number: K791987 · 1979-10-04

ApplicantEdward Weck, Inc.
Decision Date1979-10-04
Product CodeGEN
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

VASCULAR FORCEPS & CLAMPS is the device name listed in this FDA 510(k) record. The listed applicant is Edward Weck, Inc.. It received FDA 510(k) clearance on 1979-10-04 under 510(k) number K791987. 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 VASCULAR FORCEPS & CLAMPS?

VASCULAR FORCEPS & CLAMPS is a medical device that received FDA 510(k) clearance on 1979-10-04. The listed applicant is Edward Weck, Inc.. The 510(k) number is K791987.

When did VASCULAR FORCEPS & CLAMPS receive FDA 510(k) clearance?

VASCULAR FORCEPS & CLAMPS received FDA 510(k) clearance on 1979-10-04, under 510(k) number K791987.

Who is the listed applicant for VASCULAR FORCEPS & CLAMPS?

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

What is the FDA product code for VASCULAR FORCEPS & CLAMPS?

The FDA product code for VASCULAR FORCEPS & CLAMPS is GEN.

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Other records listing Edward Weck, 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.

K915378WECK TROCARK914690LM15(TM), CATALOG NUMBER - 523821K911915HEMOCLIP IIK914470PNEUMO-SEAL(TM)K911272ENDOSCOPIC NEEDLHOLDER CAT. NUMBER 114705K902108HEM-O-LOK(TM)

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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

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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