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FDA 510(k)

VERSA-STIM ELECTRODE LINE MODIFIED

K-Number: K911069 · 1991-07-16

ApplicantConmedcorp
Decision Date1991-07-16
Product CodeGXY
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

VERSA-STIM ELECTRODE LINE MODIFIED is the device name listed in this FDA 510(k) record. The listed applicant is Conmedcorp. It received FDA 510(k) clearance on 1991-07-16 under 510(k) number K911069. 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 VERSA-STIM ELECTRODE LINE MODIFIED?

VERSA-STIM ELECTRODE LINE MODIFIED is a medical device that received FDA 510(k) clearance on 1991-07-16. The listed applicant is Conmedcorp. The 510(k) number is K911069.

When did VERSA-STIM ELECTRODE LINE MODIFIED receive FDA 510(k) clearance?

VERSA-STIM ELECTRODE LINE MODIFIED received FDA 510(k) clearance on 1991-07-16, under 510(k) number K911069.

Who is the listed applicant for VERSA-STIM ELECTRODE LINE MODIFIED?

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 VERSA-STIM ELECTRODE LINE MODIFIED?

The FDA product code for VERSA-STIM ELECTRODE LINE MODIFIED 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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