FDA 510(k)

UES-30 ELECTROSURGICAL UNIT AND IT'S ASSOCIATED ACCESSORIES

K-Number: K023767 · 2002-11-29

Decision Date2002-11-29

Product CodeGEI

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

UES-30 ELECTROSURGICAL UNIT AND IT'S ASSOCIATED ACCESSORIES is the device name listed in this FDA 510(k) record. The listed applicant is The Olympus Optical Co.. It received FDA 510(k) clearance on 2002-11-29 under 510(k) number K023767. 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 UES-30 ELECTROSURGICAL UNIT AND IT'S ASSOCIATED ACCESSORIES?

UES-30 ELECTROSURGICAL UNIT AND IT'S ASSOCIATED ACCESSORIES is a medical device that received FDA 510(k) clearance on 2002-11-29. The listed applicant is The Olympus Optical Co.. The 510(k) number is K023767.

When did UES-30 ELECTROSURGICAL UNIT AND IT'S ASSOCIATED ACCESSORIES receive FDA 510(k) clearance?

UES-30 ELECTROSURGICAL UNIT AND IT'S ASSOCIATED ACCESSORIES received FDA 510(k) clearance on 2002-11-29, under 510(k) number K023767.

Who is the listed applicant for UES-30 ELECTROSURGICAL UNIT AND IT'S ASSOCIATED ACCESSORIES?

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

What is the FDA product code for UES-30 ELECTROSURGICAL UNIT AND IT'S ASSOCIATED ACCESSORIES?

The FDA product code for UES-30 ELECTROSURGICAL UNIT AND IT'S ASSOCIATED ACCESSORIES is GEI.

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Other records listing The Olympus Optical Co. as applicant

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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.