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FDA 510(k)

MODULAR DESIGN ELECTROSURGICAL LAPAROSCOPY INTR

K-Number: K920166 · 1992-11-06

ApplicantConmedcorp
Decision Date1992-11-06
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

MODULAR DESIGN ELECTROSURGICAL LAPAROSCOPY INTR is the device name listed in this FDA 510(k) record. The listed applicant is Conmedcorp. It received FDA 510(k) clearance on 1992-11-06 under 510(k) number K920166. 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 MODULAR DESIGN ELECTROSURGICAL LAPAROSCOPY INTR?

MODULAR DESIGN ELECTROSURGICAL LAPAROSCOPY INTR is a medical device that received FDA 510(k) clearance on 1992-11-06. The listed applicant is Conmedcorp. The 510(k) number is K920166.

When did MODULAR DESIGN ELECTROSURGICAL LAPAROSCOPY INTR receive FDA 510(k) clearance?

MODULAR DESIGN ELECTROSURGICAL LAPAROSCOPY INTR received FDA 510(k) clearance on 1992-11-06, under 510(k) number K920166.

Who is the listed applicant for MODULAR DESIGN ELECTROSURGICAL LAPAROSCOPY INTR?

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 MODULAR DESIGN ELECTROSURGICAL LAPAROSCOPY INTR?

The FDA product code for MODULAR DESIGN ELECTROSURGICAL LAPAROSCOPY INTR 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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