SURX RADIOFREQUENCY ELECTROSURGICAL GENERATOR SYSTEM AND ACCESSORIES (SURX LP SYSTEM)— 510(k) K011190

Name: FDA 510(k) clearance K011190
Creator: U.S. Food and Drug Administration
Published: 2002-01-08

Substantially Equivalent

Surx, Inc.

FDA 510(k) clearance K011190 for SURX RADIOFREQUENCY ELECTROSURGICAL GENERATOR SYSTEM AND ACCESSORIES (SURX LP SYSTEM), Substantially Equivalent on 2002-01-08. Applicant: Surx, Inc.. Device class: 2.

Clearance details

Applicant: Surx, Inc.
Product code: Code MUK
Device class: Class 2
Regulation: 21 CFR 878.4400
Advisory panel: General, Plastic Surgery
Date received: 2001-04-19
Decision date: 2002-01-08
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Pleasanton, CA, US

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