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FDA 510(k)

160/260 SUCTION COAGULATOR

K-Number: K830926 · 1983-06-02

ApplicantZimmer, Inc.
Decision Date1983-06-02
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

160/260 SUCTION COAGULATOR is the device name listed in this FDA 510(k) record. The listed applicant is Zimmer, Inc.. It received FDA 510(k) clearance on 1983-06-02 under 510(k) number K830926. 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 160/260 SUCTION COAGULATOR?

160/260 SUCTION COAGULATOR is a medical device that received FDA 510(k) clearance on 1983-06-02. The listed applicant is Zimmer, Inc.. The 510(k) number is K830926.

When did 160/260 SUCTION COAGULATOR receive FDA 510(k) clearance?

160/260 SUCTION COAGULATOR received FDA 510(k) clearance on 1983-06-02, under 510(k) number K830926.

Who is the listed applicant for 160/260 SUCTION COAGULATOR?

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

What is the FDA product code for 160/260 SUCTION COAGULATOR?

The FDA product code for 160/260 SUCTION COAGULATOR 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.

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