FDA 510(k)

HARRINGTON HOOK CLAMP

K-Number: K781448 · 1978-09-27

Decision Date1978-09-27

Product CodeGEN

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

HARRINGTON HOOK CLAMP is the device name listed in this FDA 510(k) record. The listed applicant is Orthopedic Equipment Co., Inc.. It received FDA 510(k) clearance on 1978-09-27 under 510(k) number K781448. 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 HARRINGTON HOOK CLAMP?

HARRINGTON HOOK CLAMP is a medical device that received FDA 510(k) clearance on 1978-09-27. The listed applicant is Orthopedic Equipment Co., Inc.. The 510(k) number is K781448.

When did HARRINGTON HOOK CLAMP receive FDA 510(k) clearance?

HARRINGTON HOOK CLAMP received FDA 510(k) clearance on 1978-09-27, under 510(k) number K781448.

Who is the listed applicant for HARRINGTON HOOK CLAMP?

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

What is the FDA product code for HARRINGTON HOOK CLAMP?

The FDA product code for HARRINGTON HOOK CLAMP is 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.