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FDA 510(k)

INSTRUMENT, MANUAL, GENERAL SURGICAL

K-Number: K925707 · 1993-05-26

ApplicantSymbiosis Corp.
Decision Date1993-05-26
Product CodeGEI
Advisory CommitteeSU
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 1993-05-26 under 510(k) number K925707. The device is classified under product code GEI. It was reviewed by the SU 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 1993-05-26. The listed applicant is Symbiosis Corp.. The 510(k) number is K925707.

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

INSTRUMENT, MANUAL, GENERAL SURGICAL received FDA 510(k) clearance on 1993-05-26, under 510(k) number K925707.

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 GEI.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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