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FDA 510(k) Applications Submitted by PHILIPPE GIRARD
FDA 510(k) Number
Submission Date
Device Name
Applicant
K172137
07/17/2017
PIEZOTOME CUBE
Satelec - Acteon Group
K163610
12/22/2016
PIEZOTOME M+, PIEZOTOME M+ Handpiece
SATALEC-ACTEON GROUP
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