Sentinelle Medical, Inc. is one of 619 FDA 510(k) medical device manufacturers from Canada in the dataset, ranked by real submission volume.
Sentinelle Medical, Inc. - FDA 510(k) Cleared Devices
Recent clearances: SENTINELLE ENDO COIL ARRAY FOR PELVIC IMAGING, VANGUARD BREAST MRI AUXILIARY TABLE WITH 16 CHANNEL COIL ARRAY FOR GE 3T MRI SYSTEM, MODEL 4000451-51, AEGIS NAVIGATION ANDA EGIS PELVIC APPLICATION
5
Total
5
Cleared
0
Denied
Sentinelle Medical, Inc. has 5 FDA 510(k) cleared medical devices. Based in Toronto, Ontario, CA.
Historical record: 5 cleared submissions from 2006 to 2011. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Sentinelle Medical, Inc. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Intertek Testing Services and Underwriters Laboratories, Inc..
FDA 510(k) Regulatory Record - Sentinelle Medical, Inc.
5 devices
Cleared
Aug 18, 2011
SENTINELLE ENDO COIL ARRAY FOR PELVIC IMAGING
Radiology
286d
Cleared
Apr 22, 2010
VANGUARD BREAST MRI AUXILIARY TABLE WITH 16 CHANNEL COIL ARRAY FOR GE 3T MRI...
Radiology
98d
Cleared
Dec 11, 2009
AEGIS NAVIGATION ANDA EGIS PELVIC APPLICATION
Radiology
14d
Cleared
Feb 09, 2007
AEGIS
Radiology
15d
Cleared
Apr 14, 2006
VANGUARD MRI AUXILIARY PATIENT TABLE WITH 4 AND 8 CHANNEL COIL ARRAY FOR GE...
Radiology
15d