FDA 510(k)

AUTOCON II 200 ELECTROSURGICAL GENERATOR

K-Number: K023924 · 2003-02-21

Decision Date2003-02-21

Product CodeGEI

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

AUTOCON II 200 ELECTROSURGICAL GENERATOR is the device name listed in this FDA 510(k) record. The listed applicant is Karl Storz Endoscopy. It received FDA 510(k) clearance on 2003-02-21 under 510(k) number K023924. 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 AUTOCON II 200 ELECTROSURGICAL GENERATOR?

AUTOCON II 200 ELECTROSURGICAL GENERATOR is a medical device that received FDA 510(k) clearance on 2003-02-21. The listed applicant is Karl Storz Endoscopy. The 510(k) number is K023924.

When did AUTOCON II 200 ELECTROSURGICAL GENERATOR receive FDA 510(k) clearance?

AUTOCON II 200 ELECTROSURGICAL GENERATOR received FDA 510(k) clearance on 2003-02-21, under 510(k) number K023924.

Who is the listed applicant for AUTOCON II 200 ELECTROSURGICAL GENERATOR?

The FDA 510(k) record lists Karl Storz Endoscopy as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for AUTOCON II 200 ELECTROSURGICAL GENERATOR?

The FDA product code for AUTOCON II 200 ELECTROSURGICAL GENERATOR 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.