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Sentinelle Medical, Inc.

Toronto, Ontario, CA

Sentinelle Medical, Inc. appears in FDA device records in Toronto, Ontario, CA. FDA records list 5 510(k) clearances between and , no PMA records and no registered establishments. As of , FDA records show no recalls for this company.

FDA records held for this company

510(k) clearances
5
PMA records
0
Recall records
0
Registered establishments
0

510(k) clearance history

FDA records hold 5 510(k) clearances for Sentinelle Medical, Inc. between 2006 and 2011. The busiest year on record is 2006, with 1. The most recent is 2011, with 1.

Clearances by year, as a table
510(k) clearance decisions for Sentinelle Medical, Inc., by decision year
YearClearances
20061
20071
20091
20101
20111
510(k) clearances on record, most recent first
K numberDeviceProduct codeDecisionDecision date
K103274SENTINELLE ENDO COIL ARRAY FOR PELVIC IMAGINGMOSSubstantially Equivalent
K100113VANGUARD BREAST MRI AUXILIARY TABLE WITH 16 CHANNEL COIL ARRAY FOR GE 3T MRI SYSTEM, MODEL 4000451-51MOSSubstantially Equivalent
K093672AEGIS NAVIGATION ANDA EGIS PELVIC APPLICATIONLLZSubstantially Equivalent
K070244AEGISLLZSubstantially Equivalent
K060873VANGUARD MRI AUXILIARY PATIENT TABLE WITH 4 AND 8 CHANNEL COIL ARRAY FOR GE SIGNA SYSTEMSMOSSubstantially Equivalent

Registered establishments

No FDA establishment registrations recorded against this company.

FDA product codes

Recall records

No recall records for this company in the ingested FDA data.

Verification record

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Data as of , FDA export datePage updated Source: openFDA, public domain