KREATIV MACH 5, MACH 5 PLUS, MACH M, MACH 6— 510(k) K980216

Name: FDA 510(k) clearance K980216
Creator: U.S. Food and Drug Administration
Published: 1998-06-16

Substantially Equivalent

Kreativ, Inc.

FDA 510(k) clearance K980216 for KREATIV MACH 5, MACH 5 PLUS, MACH M, MACH 6, Substantially Equivalent on 1998-06-16. Applicant: Kreativ, Inc.. Device class: 2.

Clearance details

Applicant: Kreativ, Inc.
Product code: Code KOJ
Device class: Class 2
Regulation: 21 CFR 872.6080
Advisory panel: Dental
Date received: 1998-01-21
Decision date: 1998-06-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Albany, OR, US

Download summary PDF View on FDA.gov ↗

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