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FDA 510(k)

MULTI USE LAPAROSCOPY ELECTROSURGICAL INSTRUMENT

K-Number: K915204 · 1992-06-04

ApplicantConmedcorp
Decision Date1992-06-04
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

MULTI USE LAPAROSCOPY ELECTROSURGICAL INSTRUMENT is the device name listed in this FDA 510(k) record. The listed applicant is Conmedcorp. It received FDA 510(k) clearance on 1992-06-04 under 510(k) number K915204. 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 MULTI USE LAPAROSCOPY ELECTROSURGICAL INSTRUMENT?

MULTI USE LAPAROSCOPY ELECTROSURGICAL INSTRUMENT is a medical device that received FDA 510(k) clearance on 1992-06-04. The listed applicant is Conmedcorp. The 510(k) number is K915204.

When did MULTI USE LAPAROSCOPY ELECTROSURGICAL INSTRUMENT receive FDA 510(k) clearance?

MULTI USE LAPAROSCOPY ELECTROSURGICAL INSTRUMENT received FDA 510(k) clearance on 1992-06-04, under 510(k) number K915204.

Who is the listed applicant for MULTI USE LAPAROSCOPY ELECTROSURGICAL INSTRUMENT?

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

What is the FDA product code for MULTI USE LAPAROSCOPY ELECTROSURGICAL INSTRUMENT?

The FDA product code for MULTI USE LAPAROSCOPY ELECTROSURGICAL INSTRUMENT is GEI.

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Related Devices (Code: 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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