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FDA 510(k)

CONMED UNIVERSAL PLUS

K-Number: K934828 · 1994-03-07

ApplicantConmedcorp
Decision Date1994-03-07
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

CONMED UNIVERSAL PLUS is the device name listed in this FDA 510(k) record. The listed applicant is Conmedcorp. It received FDA 510(k) clearance on 1994-03-07 under 510(k) number K934828. 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 CONMED UNIVERSAL PLUS?

CONMED UNIVERSAL PLUS is a medical device that received FDA 510(k) clearance on 1994-03-07. The listed applicant is Conmedcorp. The 510(k) number is K934828.

When did CONMED UNIVERSAL PLUS receive FDA 510(k) clearance?

CONMED UNIVERSAL PLUS received FDA 510(k) clearance on 1994-03-07, under 510(k) number K934828.

Who is the listed applicant for CONMED UNIVERSAL PLUS?

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 UNIVERSAL PLUS?

The FDA product code for CONMED UNIVERSAL PLUS is GEI.

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Other records listing Conmedcorp as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Related Devices (Code: GEI)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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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