FDA 510(k)

ELECTROSURGIAL INSTRUMENTS

K-Number: K932654 · 1994-02-22

Decision Date1994-02-22

Product CodeGEI

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

ELECTROSURGIAL INSTRUMENTS is the device name listed in this FDA 510(k) record. The listed applicant is Medline Industries, Inc.. It received FDA 510(k) clearance on 1994-02-22 under 510(k) number K932654. 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 ELECTROSURGIAL INSTRUMENTS?

ELECTROSURGIAL INSTRUMENTS is a medical device that received FDA 510(k) clearance on 1994-02-22. The listed applicant is Medline Industries, Inc.. The 510(k) number is K932654.

When did ELECTROSURGIAL INSTRUMENTS receive FDA 510(k) clearance?

ELECTROSURGIAL INSTRUMENTS received FDA 510(k) clearance on 1994-02-22, under 510(k) number K932654.

Who is the listed applicant for ELECTROSURGIAL INSTRUMENTS?

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

What is the FDA product code for ELECTROSURGIAL INSTRUMENTS?

The FDA product code for ELECTROSURGIAL INSTRUMENTS 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.