MODIFICATION TO SURX RADIOFREQUENCY ELECTROSURGICAL GENERATOR SYSTEM AND ACCESSORIES (SURX TV SYSTEM)— 510(k) K020126

Name: FDA 510(k) clearance K020126
Creator: U.S. Food and Drug Administration
Published: 2002-03-15

Substantially Equivalent

Surx, Inc.

FDA 510(k) clearance K020126 for MODIFICATION TO SURX RADIOFREQUENCY ELECTROSURGICAL GENERATOR SYSTEM AND ACCESSORIES (SURX TV SYSTEM), Substantially Equivalent on 2002-03-15. 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: 2002-01-15
Decision date: 2002-03-15
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Livermore, CA, US

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K020952 — SURX RF SYSTEM2002-05-30
K011190 — SURX RADIOFREQUENCY ELECTROSURGICAL GENERATOR SYSTEM AND ACCESSORIES (SURX LP SYSTEM)2002-01-08

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