FDA 510(k)

POWERSTAR BIPOLAR SCISSORS

K-Number: K973173 · 1997-10-29

Decision Date1997-10-29

Product CodeGEI

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

POWERSTAR BIPOLAR SCISSORS is the device name listed in this FDA 510(k) record. The listed applicant is ETHICON, Inc.. It received FDA 510(k) clearance on 1997-10-29 under 510(k) number K973173. 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 POWERSTAR BIPOLAR SCISSORS?

POWERSTAR BIPOLAR SCISSORS is a medical device that received FDA 510(k) clearance on 1997-10-29. The listed applicant is ETHICON, Inc.. The 510(k) number is K973173.

When did POWERSTAR BIPOLAR SCISSORS receive FDA 510(k) clearance?

POWERSTAR BIPOLAR SCISSORS received FDA 510(k) clearance on 1997-10-29, under 510(k) number K973173.

Who is the listed applicant for POWERSTAR BIPOLAR SCISSORS?

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

What is the FDA product code for POWERSTAR BIPOLAR SCISSORS?

The FDA product code for POWERSTAR BIPOLAR SCISSORS 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.