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FDA 510(k)

UNIVERSAL PLUS ES S/I INSTRUMENT

K-Number: K954056 · 1995-09-29

ApplicantConmedcorp
Decision Date1995-09-29
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

UNIVERSAL PLUS ES S/I INSTRUMENT is the device name listed in this FDA 510(k) record. The listed applicant is Conmedcorp. It received FDA 510(k) clearance on 1995-09-29 under 510(k) number K954056. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the UNIVERSAL PLUS ES S/I INSTRUMENT?

UNIVERSAL PLUS ES S/I INSTRUMENT is a medical device that received FDA 510(k) clearance on 1995-09-29. The listed applicant is Conmedcorp. The 510(k) number is K954056.

When did UNIVERSAL PLUS ES S/I INSTRUMENT receive FDA 510(k) clearance?

UNIVERSAL PLUS ES S/I INSTRUMENT received FDA 510(k) clearance on 1995-09-29, under 510(k) number K954056.

Who is the listed applicant for UNIVERSAL PLUS ES S/I INSTRUMENT?

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 UNIVERSAL PLUS ES S/I INSTRUMENT?

The FDA product code for UNIVERSAL PLUS ES S/I INSTRUMENT is GEI.

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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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