FDA 510(k)

MIS ELECTROSURGICAL ELECTRODES

K-Number: K915788 · 1992-03-13

Decision Date1992-03-13

Product CodeGEI

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

MIS ELECTROSURGICAL ELECTRODES is the device name listed in this FDA 510(k) record. The listed applicant is Beacon Laboratories, Inc.. It received FDA 510(k) clearance on 1992-03-13 under 510(k) number K915788. 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 MIS ELECTROSURGICAL ELECTRODES?

MIS ELECTROSURGICAL ELECTRODES is a medical device that received FDA 510(k) clearance on 1992-03-13. The listed applicant is Beacon Laboratories, Inc.. The 510(k) number is K915788.

When did MIS ELECTROSURGICAL ELECTRODES receive FDA 510(k) clearance?

MIS ELECTROSURGICAL ELECTRODES received FDA 510(k) clearance on 1992-03-13, under 510(k) number K915788.

Who is the listed applicant for MIS ELECTROSURGICAL ELECTRODES?

The FDA 510(k) record lists Beacon Laboratories, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MIS ELECTROSURGICAL ELECTRODES?

The FDA product code for MIS ELECTROSURGICAL ELECTRODES 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.