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FDA 510(k)

CONMED VERSA-STIM INTERFERENTIAL ELECTRODE

K-Number: K940704 · 1994-06-22

ApplicantConmedcorp
Decision Date1994-06-22
Product CodeGXY
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

CONMED VERSA-STIM INTERFERENTIAL ELECTRODE is the device name listed in this FDA 510(k) record. The listed applicant is Conmedcorp. It received FDA 510(k) clearance on 1994-06-22 under 510(k) number K940704. 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 INTERFERENTIAL ELECTRODE?

CONMED VERSA-STIM INTERFERENTIAL ELECTRODE is a medical device that received FDA 510(k) clearance on 1994-06-22. The listed applicant is Conmedcorp. The 510(k) number is K940704.

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

CONMED VERSA-STIM INTERFERENTIAL ELECTRODE received FDA 510(k) clearance on 1994-06-22, under 510(k) number K940704.

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

The FDA product code for CONMED VERSA-STIM INTERFERENTIAL ELECTRODE is 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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