PROGOLD ELECTROCOPING SYSTEM— 510(k) K980613

Name: FDA 510(k) clearance K980613
Creator: U.S. Food and Drug Administration
Published: 1998-03-09

Substantially Equivalent

Micro Dental Laboratories

FDA 510(k) clearance K980613 for PROGOLD ELECTROCOPING SYSTEM, Substantially Equivalent on 1998-03-09. Applicant: Micro Dental Laboratories. Device class: 2.

Clearance details

Applicant: Micro Dental Laboratories
Product code: Code EJT
Device class: Class 2
Regulation: 21 CFR 872.3060
Advisory panel: Dental
Date received: 1998-02-18
Decision date: 1998-03-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Dublin, CA, US

Download summary PDF View on FDA.gov ↗

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