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FDA 510(k)

CONMED SELECT ONE LAPAROSCOPY ELECTRODE

K-Number: K960808 · 1996-03-21

ApplicantConmedcorp
Decision Date1996-03-21
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

CONMED SELECT ONE LAPAROSCOPY ELECTRODE is the device name listed in this FDA 510(k) record. The listed applicant is Conmedcorp. It received FDA 510(k) clearance on 1996-03-21 under 510(k) number K960808. 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 CONMED SELECT ONE LAPAROSCOPY ELECTRODE?

CONMED SELECT ONE LAPAROSCOPY ELECTRODE is a medical device that received FDA 510(k) clearance on 1996-03-21. The listed applicant is Conmedcorp. The 510(k) number is K960808.

When did CONMED SELECT ONE LAPAROSCOPY ELECTRODE receive FDA 510(k) clearance?

CONMED SELECT ONE LAPAROSCOPY ELECTRODE received FDA 510(k) clearance on 1996-03-21, under 510(k) number K960808.

Who is the listed applicant for CONMED SELECT ONE LAPAROSCOPY ELECTRODE?

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 CONMED SELECT ONE LAPAROSCOPY ELECTRODE?

The FDA product code for CONMED SELECT ONE LAPAROSCOPY ELECTRODE is GEI.

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Related Devices (Code: GEI)

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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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