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FDA 510(k)

VERSASTIM, PERFOAMAX, SURGI-STIM, FASTSTART

K-Number: K041953 · 2004-08-09

ApplicantConmedcorp
Decision Date2004-08-09
Product CodeGXY
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

VERSASTIM, PERFOAMAX, SURGI-STIM, FASTSTART is the device name listed in this FDA 510(k) record. The listed applicant is Conmedcorp. It received FDA 510(k) clearance on 2004-08-09 under 510(k) number K041953. 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 VERSASTIM, PERFOAMAX, SURGI-STIM, FASTSTART?

VERSASTIM, PERFOAMAX, SURGI-STIM, FASTSTART is a medical device that received FDA 510(k) clearance on 2004-08-09. The listed applicant is Conmedcorp. The 510(k) number is K041953.

When did VERSASTIM, PERFOAMAX, SURGI-STIM, FASTSTART receive FDA 510(k) clearance?

VERSASTIM, PERFOAMAX, SURGI-STIM, FASTSTART received FDA 510(k) clearance on 2004-08-09, under 510(k) number K041953.

Who is the listed applicant for VERSASTIM, PERFOAMAX, SURGI-STIM, FASTSTART?

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 VERSASTIM, PERFOAMAX, SURGI-STIM, FASTSTART?

The FDA product code for VERSASTIM, PERFOAMAX, SURGI-STIM, FASTSTART 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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