BONART ART-E1 ELECTROSURGERY UNIT— 510(k) K020080

Name: FDA 510(k) clearance K020080
Creator: U.S. Food and Drug Administration
Published: 2002-02-19

Substantially Equivalent

Diagnostic Data, Inc.

FDA 510(k) clearance K020080 for BONART ART-E1 ELECTROSURGERY UNIT, Substantially Equivalent on 2002-02-19. Applicant: Diagnostic Data, Inc.. Device class: 2.

Clearance details

Applicant: Diagnostic Data, Inc.
Product code: Code EKZ
Device class: Class 2
Regulation: 21 CFR 872.4920
Advisory panel: Dental
Date received: 2002-01-09
Decision date: 2002-02-19
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Upland, CA, US

Download summary PDF View on FDA.gov ↗

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