MILLENNIUM EDITION 2000 ACCELERATED ELECTROFORMING SYSTEM— 510(k) K002675

Name: FDA 510(k) clearance K002675
Creator: U.S. Food and Drug Administration
Published: 2000-10-25

Substantially Equivalent

Product Development Industries, Inc.

FDA 510(k) clearance K002675 for MILLENNIUM EDITION 2000 ACCELERATED ELECTROFORMING SYSTEM, Substantially Equivalent on 2000-10-25. Applicant: Product Development Industries, Inc.. Device class: 2.

Clearance details

Applicant: Product Development Industries, Inc.
Product code: Code EJT
Device class: Class 2
Regulation: 21 CFR 872.3060
Advisory panel: Dental
Date received: 2000-08-28
Decision date: 2000-10-25
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Tucson, AZ, US

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