PIEZOTOME SOLO— 510(k) K112188

Substantially Equivalent

Satelec - Acteon, Inc.

FDA 510(k) clearance K112188 for PIEZOTOME SOLO, Substantially Equivalent on 2012-02-03. Applicant: Satelec - Acteon, Inc..

Clearance details

Applicant: Satelec - Acteon, Inc.
Product code: Code DZI
Advisory panel: Dental
Date received: 2011-07-29
Decision date: 2012-02-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mt. Laurel, NJ, US

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