T1 CONTROL HIGH SPEED DENTAL HANDPIECE— 510(k) K965238

Name: FDA 510(k) clearance K965238
Creator: U.S. Food and Drug Administration
Published: 1997-03-19

Substantially Equivalent

Siemens AG

FDA 510(k) clearance K965238 for T1 CONTROL HIGH SPEED DENTAL HANDPIECE, Substantially Equivalent on 1997-03-19. Applicant: Siemens AG. Device class: 1.

Clearance details

Applicant: Siemens AG
Product code: Code EFA
Device class: Class 1
Regulation: 21 CFR 872.4200
Advisory panel: Dental
Date received: 1996-12-31
Decision date: 1997-03-19
Decision: Substantially Equivalent
Clearance type: Traditional
Location: North Attleboro, MA, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code EFA

view all

K192809 — Dental Handpiece2020-08-25
K163239 — SMARTmatic2017-03-17
K143465 — MASTERmatic LUX2015-04-09
K101172 — RDT3 HANDPIECE HEAD MODEL RDT32010-07-27
K093894 — ANTHOGYR IMPULSION IMPLANTOLOGY CONTRA-ANGLE2010-03-03

More clearances from Siemens AG

view all

K150843 — syngo®.via (version VB10A)2015-04-24
K123375 — SYNGO.VIA2012-11-20
K110366 — SYNGO.CT CARDIAC FUNCTION2011-04-12
K071310 — SYNGO CT ONCOLOGY SOFTWARE PACKAGE2007-06-08
K063507 — SYNGO NEURO PBV CT2006-11-30

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