Hitachi Aloka Medical, Ltd. - FDA 510(k) Cleared Devices
Recent clearances: NOBLUS DIAGNOSTIC ULTRASOUND SCANNER, INTRA-OPERATIVE ULTRASOUND TRANSDUCER, PROSOUND F75 DIAGNOSTIC ULTRASOUND SYSTEM
6
Total
6
Cleared
0
Denied
FDA 510(k) Regulatory Record - Hitachi Aloka Medical, Ltd. Radiology ✕
6 devices
Cleared
Jan 14, 2015
NOBLUS DIAGNOSTIC ULTRASOUND SCANNER
Radiology
142d
Cleared
Jun 11, 2014
INTRA-OPERATIVE ULTRASOUND TRANSDUCER
Radiology
69d
Cleared
Apr 16, 2014
PROSOUND F75 DIAGNOSTIC ULTRASOUND SYSTEM
Radiology
35d
Cleared
Apr 05, 2013
NOBLUS ULTRASOUND DIAGNOSTIC SYSTEM
Radiology
57d
Cleared
Jan 18, 2013
PROSOUND F75 DIAGNOSTIC ULTRASOUND SYSTEM
Radiology
37d
Cleared
Sep 26, 2012
PROSOUND F37 DIAGNOSTIC ULTRASOUND SYSTEM, MODEL: PROSOUND F37
Radiology
55d