Hitachi Aloka Medical, Ltd. is one of 18478 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
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
Hitachi Aloka Medical, Ltd. has 6 FDA 510(k) cleared medical devices. Based in Wallingford, US.
Historical record: 6 cleared submissions from 2012 to 2015. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Hitachi Aloka Medical, Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Tuv Rheinland of North America, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Hitachi Aloka Medical, Ltd.
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