Siemens Ultrasound, Inc. - FDA 510(k) Cleared Devices
8
Total
8
Cleared
0
Denied
Siemens Ultrasound, Inc. has 8 FDA 510(k) cleared medical devices. Based in Pleasanton, US.
Historical record: 8 cleared submissions from 1989 to 1991. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Siemens Ultrasound, Inc. Filter by specialty or product code using the sidebar.
8 devices
Cleared
Dec 02, 1991
SI-450/ILUS (INTRALUMINAL ULTRASOUND)
Radiology
187d
Cleared
Dec 02, 1991
SIEMENS SI-400
Radiology
84d
Cleared
Jun 17, 1991
SI-1200 / ILUS
Radiology
90d
Cleared
Mar 21, 1991
SIEMENS SONOLINE SI-450, OB/GYN,ENT,DENTAL DEVICES
Radiology
203d
Cleared
Mar 15, 1991
7.5 MHZ PEDIATRIC TRANSESOPHAGEAL ECHO (TEE) TRANS
Radiology
35d
Cleared
Mar 15, 1991
5 MHZ ADULT/PEDI TRANSESOPHAGEAL ECHO(TEE) TRANSDU
Radiology
28d
Cleared
Oct 05, 1989
SONOLINE CF
Radiology
204d
Cleared
Jun 05, 1989
SIEMENS TRANSESOPHAGEAL ECHO TEE TRANSDUCER
Radiology
90d