DeviceClearance

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.. Device class: 2.

Clearance details

Applicant
Satelec - Acteon, Inc.
Product code
Code DZI
Device class
Class 2
Regulation
21 CFR 872.4120
Advisory panel
Dental
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Mt. Laurel, NJ, US
Download summary PDFView on FDA.gov ↗

Recent devices under product code DZI

view all

Data sourced from openFDA. This site is unofficial and independent of the FDA.