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FDA 510(k)

CASTROVIEJO VASCULAR NEEDLEHOLDER 538425

K-Number: K792309 · 1979-11-30

ApplicantEdward Weck, Inc.
Decision Date1979-11-30
Product CodeGEN
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

CASTROVIEJO VASCULAR NEEDLEHOLDER 538425 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 1979-11-30 under 510(k) number K792309. 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 CASTROVIEJO VASCULAR NEEDLEHOLDER 538425?

CASTROVIEJO VASCULAR NEEDLEHOLDER 538425 is a medical device that received FDA 510(k) clearance on 1979-11-30. The listed applicant is Edward Weck, Inc.. The 510(k) number is K792309.

When did CASTROVIEJO VASCULAR NEEDLEHOLDER 538425 receive FDA 510(k) clearance?

CASTROVIEJO VASCULAR NEEDLEHOLDER 538425 received FDA 510(k) clearance on 1979-11-30, under 510(k) number K792309.

Who is the listed applicant for CASTROVIEJO VASCULAR NEEDLEHOLDER 538425?

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 CASTROVIEJO VASCULAR NEEDLEHOLDER 538425?

The FDA product code for CASTROVIEJO VASCULAR NEEDLEHOLDER 538425 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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