FDA 510(k)

LAPAROSCOPIC ELECTRODE WITH LAVAGE AND SUCTION

K-Number: K911476 · 1991-07-02

ApplicantUnited States Endoscopy Group, Inc.

Decision Date1991-07-02

Product CodeGEI

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

LAPAROSCOPIC ELECTRODE WITH LAVAGE AND SUCTION is the device name listed in this FDA 510(k) record. The listed applicant is United States Endoscopy Group, Inc.. It received FDA 510(k) clearance on 1991-07-02 under 510(k) number K911476. 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 LAPAROSCOPIC ELECTRODE WITH LAVAGE AND SUCTION?

LAPAROSCOPIC ELECTRODE WITH LAVAGE AND SUCTION is a medical device that received FDA 510(k) clearance on 1991-07-02. The listed applicant is United States Endoscopy Group, Inc.. The 510(k) number is K911476.

When did LAPAROSCOPIC ELECTRODE WITH LAVAGE AND SUCTION receive FDA 510(k) clearance?

LAPAROSCOPIC ELECTRODE WITH LAVAGE AND SUCTION received FDA 510(k) clearance on 1991-07-02, under 510(k) number K911476.

Who is the listed applicant for LAPAROSCOPIC ELECTRODE WITH LAVAGE AND SUCTION?

The FDA 510(k) record lists United States Endoscopy Group, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LAPAROSCOPIC ELECTRODE WITH LAVAGE AND SUCTION?

The FDA product code for LAPAROSCOPIC ELECTRODE WITH LAVAGE AND SUCTION 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.