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FDA 510(k)

HOOK SURGICAL INSTRUMENT

K-Number: K920599 · 1992-07-15

ApplicantOrigin Medsystems, Inc.
Decision Date1992-07-15
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

HOOK SURGICAL INSTRUMENT is the device name listed in this FDA 510(k) record. The listed applicant is Origin Medsystems, Inc.. It received FDA 510(k) clearance on 1992-07-15 under 510(k) number K920599. The device is classified under product code GCJ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HOOK SURGICAL INSTRUMENT?

HOOK SURGICAL INSTRUMENT is a medical device that received FDA 510(k) clearance on 1992-07-15. The listed applicant is Origin Medsystems, Inc.. The 510(k) number is K920599.

When did HOOK SURGICAL INSTRUMENT receive FDA 510(k) clearance?

HOOK SURGICAL INSTRUMENT received FDA 510(k) clearance on 1992-07-15, under 510(k) number K920599.

Who is the listed applicant for HOOK SURGICAL INSTRUMENT?

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

What is the FDA product code for HOOK SURGICAL INSTRUMENT?

The FDA product code for HOOK SURGICAL INSTRUMENT is GCJ.

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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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