PROTECH DENT— 510(k) K121272

Name: FDA 510(k) clearance K121272
Creator: U.S. Food and Drug Administration
Published: 2012-10-15

Substantially Equivalent

Akervall Technologies, Inc.

FDA 510(k) clearance K121272 for PROTECH DENT, Substantially Equivalent on 2012-10-15. Applicant: Akervall Technologies, Inc.. Device class: Unclassified.

Clearance details

Applicant: Akervall Technologies, Inc.
Product code: Code OBR
Device class: Unclassified
Advisory panel: Unknown
Date received: 2012-04-27
Decision date: 2012-10-15
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Ann Arbor, MI, US

Download summary PDF View on FDA.gov ↗

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