WALLACH QUANTUM 500 ELECTROSURGICAL GENERATOR— 510(k) K000768

Name: FDA 510(k) clearance K000768
Creator: U.S. Food and Drug Administration
Published: 2000-04-11

Substantially Equivalent

Wallach Surgical Devices, Inc.

FDA 510(k) clearance K000768 for WALLACH QUANTUM 500 ELECTROSURGICAL GENERATOR, Substantially Equivalent on 2000-04-11. Applicant: Wallach Surgical Devices, Inc.. Device class: 2.

Clearance details

Applicant: Wallach Surgical Devices, Inc.
Product code: Code EKZ
Device class: Class 2
Regulation: 21 CFR 872.4920
Advisory panel: Dental
Date received: 2000-03-09
Decision date: 2000-04-11
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Orange, CT, US

Download summary PDF View on FDA.gov ↗

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