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FDA 510(k)

INSTRUMENT, MANUAL, GENERAL SURGICAL

K-Number: K922571 · 1992-08-11

ApplicantSymbiosis Corp.
Decision Date1992-08-11
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

INSTRUMENT, MANUAL, GENERAL SURGICAL is the device name listed in this FDA 510(k) record. The listed applicant is Symbiosis Corp.. It received FDA 510(k) clearance on 1992-08-11 under 510(k) number K922571. 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 INSTRUMENT, MANUAL, GENERAL SURGICAL?

INSTRUMENT, MANUAL, GENERAL SURGICAL is a medical device that received FDA 510(k) clearance on 1992-08-11. The listed applicant is Symbiosis Corp.. The 510(k) number is K922571.

When did INSTRUMENT, MANUAL, GENERAL SURGICAL receive FDA 510(k) clearance?

INSTRUMENT, MANUAL, GENERAL SURGICAL received FDA 510(k) clearance on 1992-08-11, under 510(k) number K922571.

Who is the listed applicant for INSTRUMENT, MANUAL, GENERAL SURGICAL?

The FDA 510(k) record lists Symbiosis Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for INSTRUMENT, MANUAL, GENERAL SURGICAL?

The FDA product code for INSTRUMENT, MANUAL, GENERAL SURGICAL 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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