FDA 510(k)

HEAT SCISSORS GENERATOR SET AND HEAT SCISSORS HANDPIECE

K-Number: K024138 · 2003-03-12

Decision Date2003-03-12

Product CodeGEI

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

HEAT SCISSORS GENERATOR SET AND HEAT SCISSORS HANDPIECE is the device name listed in this FDA 510(k) record. The listed applicant is Olympus Optical Co., Ltd.. It received FDA 510(k) clearance on 2003-03-12 under 510(k) number K024138. 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 HEAT SCISSORS GENERATOR SET AND HEAT SCISSORS HANDPIECE?

HEAT SCISSORS GENERATOR SET AND HEAT SCISSORS HANDPIECE is a medical device that received FDA 510(k) clearance on 2003-03-12. The listed applicant is Olympus Optical Co., Ltd.. The 510(k) number is K024138.

When did HEAT SCISSORS GENERATOR SET AND HEAT SCISSORS HANDPIECE receive FDA 510(k) clearance?

HEAT SCISSORS GENERATOR SET AND HEAT SCISSORS HANDPIECE received FDA 510(k) clearance on 2003-03-12, under 510(k) number K024138.

Who is the listed applicant for HEAT SCISSORS GENERATOR SET AND HEAT SCISSORS HANDPIECE?

The FDA 510(k) record lists Olympus Optical Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for HEAT SCISSORS GENERATOR SET AND HEAT SCISSORS HANDPIECE?

The FDA product code for HEAT SCISSORS GENERATOR SET AND HEAT SCISSORS HANDPIECE 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.