DZH — Saw, Bone, Ac-Powered Class II

FDA Device Classification

FDA product code DZH covers "Saw, Bone, Ac-Powered", a Class II medical device regulated under 21 CFR 872.4120. Submissions are reviewed by the Dental panel. At least 4 recent 510(k) clearances have been granted under this product code.

Classification Details

Product Code
DZH
Device Class
Class II
Regulation Number
872.4120
Submission Type
Review Panel
DE
Medical Specialty
Dental
Implant
No

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
K031793dentatus usaDENTATUS OSCIOMATNovember 13, 2003
K935443osada electric coADD LINE DEVICES(PARTS) ELECTRIC HANDPIECE SYSTEMSSeptember 20, 1994
K760958american safety equipmentSURGICAL OSCILLATING SAWNovember 16, 1976
K760957american safety equipmentSURGICAL RECIPROCATING SAWNovember 15, 1976