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FDA 510(k)

CONMED MODULAR DESIGN ELECTROSURGICAL LAPROSCOPY INSTRUMENTS

K-Number: K934916 · 1994-05-05

ApplicantConmedcorp
Decision Date1994-05-05
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

CONMED MODULAR DESIGN ELECTROSURGICAL LAPROSCOPY INSTRUMENTS is the device name listed in this FDA 510(k) record. The listed applicant is Conmedcorp. It received FDA 510(k) clearance on 1994-05-05 under 510(k) number K934916. The device is classified under product code GCJ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CONMED MODULAR DESIGN ELECTROSURGICAL LAPROSCOPY INSTRUMENTS?

CONMED MODULAR DESIGN ELECTROSURGICAL LAPROSCOPY INSTRUMENTS is a medical device that received FDA 510(k) clearance on 1994-05-05. The listed applicant is Conmedcorp. The 510(k) number is K934916.

When did CONMED MODULAR DESIGN ELECTROSURGICAL LAPROSCOPY INSTRUMENTS receive FDA 510(k) clearance?

CONMED MODULAR DESIGN ELECTROSURGICAL LAPROSCOPY INSTRUMENTS received FDA 510(k) clearance on 1994-05-05, under 510(k) number K934916.

Who is the listed applicant for CONMED MODULAR DESIGN ELECTROSURGICAL LAPROSCOPY INSTRUMENTS?

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 MODULAR DESIGN ELECTROSURGICAL LAPROSCOPY INSTRUMENTS?

The FDA product code for CONMED MODULAR DESIGN ELECTROSURGICAL LAPROSCOPY INSTRUMENTS is GCJ.

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Related Devices (Code: GCJ)

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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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