FDA 510(k)

ENDO WINDOW HIGH FREQUENCY ELECTROCAUTERY DEVICE, MODEL EW018

K-Number: K021266 · 2002-09-27

Decision Date2002-09-27

Product CodeKNS

Advisory CommitteeGU

DecisionSubstantially Equivalent

Device Summary

ENDO WINDOW HIGH FREQUENCY ELECTROCAUTERY DEVICE, MODEL EW018 is the device name listed in this FDA 510(k) record. The listed applicant is Ethicon Endo-Surgery, Inc.. It received FDA 510(k) clearance on 2002-09-27 under 510(k) number K021266. The device is classified under product code KNS. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ENDO WINDOW HIGH FREQUENCY ELECTROCAUTERY DEVICE, MODEL EW018?

ENDO WINDOW HIGH FREQUENCY ELECTROCAUTERY DEVICE, MODEL EW018 is a medical device that received FDA 510(k) clearance on 2002-09-27. The listed applicant is Ethicon Endo-Surgery, Inc.. The 510(k) number is K021266.

When did ENDO WINDOW HIGH FREQUENCY ELECTROCAUTERY DEVICE, MODEL EW018 receive FDA 510(k) clearance?

ENDO WINDOW HIGH FREQUENCY ELECTROCAUTERY DEVICE, MODEL EW018 received FDA 510(k) clearance on 2002-09-27, under 510(k) number K021266.

Who is the listed applicant for ENDO WINDOW HIGH FREQUENCY ELECTROCAUTERY DEVICE, MODEL EW018?

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

What is the FDA product code for ENDO WINDOW HIGH FREQUENCY ELECTROCAUTERY DEVICE, MODEL EW018?

The FDA product code for ENDO WINDOW HIGH FREQUENCY ELECTROCAUTERY DEVICE, MODEL EW018 is KNS.

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Other records listing Ethicon Endo-Surgery, Inc. as applicant

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Related Devices (Code: KNS)

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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.