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FDA 510(k)

MONOPOLAR ELECTRODES AND CABLES

K-Number: K992485 · 1999-08-27

ApplicantUs Endo, Inc.
Decision Date1999-08-27
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

MONOPOLAR ELECTRODES AND CABLES is the device name listed in this FDA 510(k) record. The listed applicant is Us Endo, Inc.. It received FDA 510(k) clearance on 1999-08-27 under 510(k) number K992485. 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 MONOPOLAR ELECTRODES AND CABLES?

MONOPOLAR ELECTRODES AND CABLES is a medical device that received FDA 510(k) clearance on 1999-08-27. The listed applicant is Us Endo, Inc.. The 510(k) number is K992485.

When did MONOPOLAR ELECTRODES AND CABLES receive FDA 510(k) clearance?

MONOPOLAR ELECTRODES AND CABLES received FDA 510(k) clearance on 1999-08-27, under 510(k) number K992485.

Who is the listed applicant for MONOPOLAR ELECTRODES AND CABLES?

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

What is the FDA product code for MONOPOLAR ELECTRODES AND CABLES?

The FDA product code for MONOPOLAR ELECTRODES AND CABLES 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.

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