FDA 510(k)

QUAD BIPOLAR LAPAROSCOPIC COAGULATING AND CUTTING INSTRUMENT

K-Number: K992186 · 1999-07-30

Decision Date1999-07-30

Product CodeGEI

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

QUAD BIPOLAR LAPAROSCOPIC COAGULATING AND CUTTING INSTRUMENT is the device name listed in this FDA 510(k) record. The listed applicant is Conmedcorp. It received FDA 510(k) clearance on 1999-07-30 under 510(k) number K992186. 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 QUAD BIPOLAR LAPAROSCOPIC COAGULATING AND CUTTING INSTRUMENT?

QUAD BIPOLAR LAPAROSCOPIC COAGULATING AND CUTTING INSTRUMENT is a medical device that received FDA 510(k) clearance on 1999-07-30. The listed applicant is Conmedcorp. The 510(k) number is K992186.

When did QUAD BIPOLAR LAPAROSCOPIC COAGULATING AND CUTTING INSTRUMENT receive FDA 510(k) clearance?

QUAD BIPOLAR LAPAROSCOPIC COAGULATING AND CUTTING INSTRUMENT received FDA 510(k) clearance on 1999-07-30, under 510(k) number K992186.

Who is the listed applicant for QUAD BIPOLAR LAPAROSCOPIC COAGULATING AND CUTTING 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 QUAD BIPOLAR LAPAROSCOPIC COAGULATING AND CUTTING INSTRUMENT?

The FDA product code for QUAD BIPOLAR LAPAROSCOPIC COAGULATING AND CUTTING INSTRUMENT is GEI.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.