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FDA 510(k)

CARROLL TENDON RETRIEVER

K-Number: K772393 · 1978-05-09

ApplicantEdward Weck, Inc.
Decision Date1978-05-09
Product CodeGEN
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

CARROLL TENDON RETRIEVER 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 1978-05-09 under 510(k) number K772393. 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 CARROLL TENDON RETRIEVER?

CARROLL TENDON RETRIEVER is a medical device that received FDA 510(k) clearance on 1978-05-09. The listed applicant is Edward Weck, Inc.. The 510(k) number is K772393.

When did CARROLL TENDON RETRIEVER receive FDA 510(k) clearance?

CARROLL TENDON RETRIEVER received FDA 510(k) clearance on 1978-05-09, under 510(k) number K772393.

Who is the listed applicant for CARROLL TENDON RETRIEVER?

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 CARROLL TENDON RETRIEVER?

The FDA product code for CARROLL TENDON RETRIEVER 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)

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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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