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FDA 510(k)

CONMED VERSA STEM NEUROMUSCULAR STIMULATION/TENS

K-Number: K944603 · 1994-12-15

ApplicantConmedcorp
Decision Date1994-12-15
Product CodeGXY
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

CONMED VERSA STEM NEUROMUSCULAR STIMULATION/TENS is the device name listed in this FDA 510(k) record. The listed applicant is Conmedcorp. It received FDA 510(k) clearance on 1994-12-15 under 510(k) number K944603. 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 STEM NEUROMUSCULAR STIMULATION/TENS?

CONMED VERSA STEM NEUROMUSCULAR STIMULATION/TENS is a medical device that received FDA 510(k) clearance on 1994-12-15. The listed applicant is Conmedcorp. The 510(k) number is K944603.

When did CONMED VERSA STEM NEUROMUSCULAR STIMULATION/TENS receive FDA 510(k) clearance?

CONMED VERSA STEM NEUROMUSCULAR STIMULATION/TENS received FDA 510(k) clearance on 1994-12-15, under 510(k) number K944603.

Who is the listed applicant for CONMED VERSA STEM NEUROMUSCULAR STIMULATION/TENS?

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 STEM NEUROMUSCULAR STIMULATION/TENS?

The FDA product code for CONMED VERSA STEM NEUROMUSCULAR STIMULATION/TENS 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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