FDA 510(k)

UNIVERSALPLUS LAPAROSCOPIC ABC/ELECTROSURGICAL ELECTRODE

K-Number: K973890 · 1998-01-02

Decision Date1998-01-02

Product CodeGEI

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

UNIVERSALPLUS LAPAROSCOPIC ABC/ELECTROSURGICAL ELECTRODE is the device name listed in this FDA 510(k) record. The listed applicant is Conmedcorp. It received FDA 510(k) clearance on 1998-01-02 under 510(k) number K973890. 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 UNIVERSALPLUS LAPAROSCOPIC ABC/ELECTROSURGICAL ELECTRODE?

UNIVERSALPLUS LAPAROSCOPIC ABC/ELECTROSURGICAL ELECTRODE is a medical device that received FDA 510(k) clearance on 1998-01-02. The listed applicant is Conmedcorp. The 510(k) number is K973890.

When did UNIVERSALPLUS LAPAROSCOPIC ABC/ELECTROSURGICAL ELECTRODE receive FDA 510(k) clearance?

UNIVERSALPLUS LAPAROSCOPIC ABC/ELECTROSURGICAL ELECTRODE received FDA 510(k) clearance on 1998-01-02, under 510(k) number K973890.

Who is the listed applicant for UNIVERSALPLUS LAPAROSCOPIC ABC/ELECTROSURGICAL ELECTRODE?

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 UNIVERSALPLUS LAPAROSCOPIC ABC/ELECTROSURGICAL ELECTRODE?

The FDA product code for UNIVERSALPLUS LAPAROSCOPIC ABC/ELECTROSURGICAL ELECTRODE 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.