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FDA 510(k)

SINGLE USE LAPAROSCOPY ELECTROSURGICAL INSTRUMENT

K-Number: K914120 · 1991-10-30

ApplicantConmedcorp
Decision Date1991-10-30
Product CodeGCI
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

SINGLE USE LAPAROSCOPY ELECTROSURGICAL INSTRUMENT is the device name listed in this FDA 510(k) record. The listed applicant is Conmedcorp. It received FDA 510(k) clearance on 1991-10-30 under 510(k) number K914120. The device is classified under product code GCI. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SINGLE USE LAPAROSCOPY ELECTROSURGICAL INSTRUMENT?

SINGLE USE LAPAROSCOPY ELECTROSURGICAL INSTRUMENT is a medical device that received FDA 510(k) clearance on 1991-10-30. The listed applicant is Conmedcorp. The 510(k) number is K914120.

When did SINGLE USE LAPAROSCOPY ELECTROSURGICAL INSTRUMENT receive FDA 510(k) clearance?

SINGLE USE LAPAROSCOPY ELECTROSURGICAL INSTRUMENT received FDA 510(k) clearance on 1991-10-30, under 510(k) number K914120.

Who is the listed applicant for SINGLE USE LAPAROSCOPY ELECTROSURGICAL 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 SINGLE USE LAPAROSCOPY ELECTROSURGICAL INSTRUMENT?

The FDA product code for SINGLE USE LAPAROSCOPY ELECTROSURGICAL INSTRUMENT is GCI.

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Other records listing Conmedcorp as applicant

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Related Devices (Code: GCI)

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.

K021747DEGALL LAPAROSCOPIC GALLBLADDER EXTRACTORSurgicon, Inc.K003222MODIFICATION TO HERMES OPERATING ROOM CONTROL CENTERComputer Motion, Inc.K001362KARL STORZ 3D VIDEO SYSTEMKarl Storz Imaging, Inc.K933515BOOTY ENDOSCOPE WARMERT-Med, Inc.K930302BIRTCHER SURE CLEAN INSTRUMENT SYSTEMBirtcher Medical Systems, Inc.K930496GI-1090,1095,1080,1085,1086,1088, ENDO. CLAMPSBirtcher Medical Systems, Inc.

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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