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FDA 510(k)

PROTHESIS, METACARPAL

K-Number: K781937 · 1979-01-17

ApplicantCutter Laboratories, Inc.
Decision Date1979-01-17
Product Code
DecisionSubstantially Equivalent

Device Summary

PROTHESIS, METACARPAL is the device name listed in this FDA 510(k) record. The listed applicant is Cutter Laboratories, Inc.. It received FDA 510(k) clearance on 1979-01-17 under 510(k) number K781937. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PROTHESIS, METACARPAL?

PROTHESIS, METACARPAL is a medical device that received FDA 510(k) clearance on 1979-01-17. The listed applicant is Cutter Laboratories, Inc.. The 510(k) number is K781937.

When did PROTHESIS, METACARPAL receive FDA 510(k) clearance?

PROTHESIS, METACARPAL received FDA 510(k) clearance on 1979-01-17, under 510(k) number K781937.

Who is the listed applicant for PROTHESIS, METACARPAL?

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

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Other records listing Cutter 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.

K861315HYPERBARIC PENETRATION EXTENSION SETK854106BAYSILEXK842324PERFOURMK834106INTRAVENOUS INFUSION CONTROLLERK832237ORTHOPEDIC CASTING TAPE MAXCASTK823214DOSIMETRIC RELEASE PROGRAM - ADMIN. SET

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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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