VELOPEX AQUACUT FLUID ABRASION UNIT— 510(k) K024105

Name: FDA 510(k) clearance K024105
Creator: U.S. Food and Drug Administration
Published: 2003-10-09

Substantially Equivalent

Velopex International, Inc.

FDA 510(k) clearance K024105 for VELOPEX AQUACUT FLUID ABRASION UNIT, Substantially Equivalent on 2003-10-09. Applicant: Velopex International, Inc.. Device class: 2.

Clearance details

Applicant: Velopex International, Inc.
Product code: Code KOJ
Device class: Class 2
Regulation: 21 CFR 872.6080
Advisory panel: Dental
Date received: 2002-12-13
Decision date: 2003-10-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: St. Cloud, FL, US

Download summary PDF View on FDA.gov ↗

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