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FDA 510(k)

CONMED VERSA-STIM NEUROMUSCULAR STIMULATION ELECTRODE

K-Number: K936101 · 1994-06-30

ApplicantConmedcorp
Decision Date1994-06-30
Product CodeGXY
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

CONMED VERSA-STIM NEUROMUSCULAR STIMULATION ELECTRODE is the device name listed in this FDA 510(k) record. The listed applicant is Conmedcorp. It received FDA 510(k) clearance on 1994-06-30 under 510(k) number K936101. The device is classified under product code GXY. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CONMED VERSA-STIM NEUROMUSCULAR STIMULATION ELECTRODE?

CONMED VERSA-STIM NEUROMUSCULAR STIMULATION ELECTRODE is a medical device that received FDA 510(k) clearance on 1994-06-30. The listed applicant is Conmedcorp. The 510(k) number is K936101.

When did CONMED VERSA-STIM NEUROMUSCULAR STIMULATION ELECTRODE receive FDA 510(k) clearance?

CONMED VERSA-STIM NEUROMUSCULAR STIMULATION ELECTRODE received FDA 510(k) clearance on 1994-06-30, under 510(k) number K936101.

Who is the listed applicant for CONMED VERSA-STIM NEUROMUSCULAR STIMULATION 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 VERSA-STIM NEUROMUSCULAR STIMULATION ELECTRODE?

The FDA product code for CONMED VERSA-STIM NEUROMUSCULAR STIMULATION ELECTRODE is GXY.

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Related Devices (Code: GXY)

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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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