PREPTECH(TM) 200 CAVITY PREPARATION SYSTEM— 510(k) K974655

Name: FDA 510(k) clearance K974655
Creator: U.S. Food and Drug Administration
Published: 1998-07-09

Substantially Equivalent

Prep Technology Corp.

FDA 510(k) clearance K974655 for PREPTECH(TM) 200 CAVITY PREPARATION SYSTEM, Substantially Equivalent on 1998-07-09. Applicant: Prep Technology Corp.. Device class: 2.

Clearance details

Applicant: Prep Technology Corp.
Product code: Code KOJ
Device class: Class 2
Regulation: 21 CFR 872.6080
Advisory panel: Dental
Date received: 1997-12-15
Decision date: 1998-07-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Freemont, CA, US

Download summary PDF View on FDA.gov ↗

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