510(k) K965238

T1 CONTROL HIGH SPEED DENTAL HANDPIECE by Siemens AG — Product Code EFA

K965238 is an FDA 510(k) premarket notification submitted by Siemens AG for the device "T1 CONTROL HIGH SPEED DENTAL HANDPIECE". The FDA issued a decision of Substantially Equivalent on March 19, 1997. The device falls under product code EFA (Handpiece, Belt And/Or Gear Driven, Dental), a Class I device regulated under 21 CFR 872.4200. Siemens AG has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
March 19, 1997
Date Received
December 31, 1996
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Handpiece, Belt And/Or Gear Driven, Dental
Device Class
Class I
Regulation Number
872.4200
Review Panel
DE
Submission Type