ETHICON ENDO-SURGERY ENSEAL G2 CORDLESS TISSUE SEALERS— 510(k) K123212

Name: FDA 510(k) clearance K123212
Creator: U.S. Food and Drug Administration
Published: 2013-03-08

Substantially Equivalent

Ethicon Endo-Surgery, LLC

FDA 510(k) clearance K123212 for ETHICON ENDO-SURGERY ENSEAL G2 CORDLESS TISSUE SEALERS, Substantially Equivalent on 2013-03-08. Applicant: Ethicon Endo-Surgery, LLC. Device class: 2.

Clearance details

Applicant: Ethicon Endo-Surgery, LLC
Product code: Code PDG
Device class: Class 2
Regulation: 21 CFR 878.4400
Advisory panel: General, Plastic Surgery
Date received: 2012-10-15
Decision date: 2013-03-08
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Cincinnati, OH, US

Download summary PDF View on FDA.gov ↗

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