Teratech Corp. is one of 18478 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Teratech Corp. - FDA 510(k) Cleared Devices
Recent clearances: Terason uSmart3200T Ultrasound System, Terason uSmart3300 Ultrasound System, TERASON USMART3300 ULTRASOUND SYSTEM
17
Total
17
Cleared
0
Denied
Teratech Corp. has 17 FDA 510(k) cleared radiology devices. Based in Saratoga, US.
Historical record: 17 cleared submissions from 1999 to 2015.
Browse the complete list of FDA 510(k) cleared radiology devices from this manufacturer. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Regulatory Technology Services, LLC, Tuv Product Service, Inc. and Tuv America, Inc..
FDA 510(k) Regulatory Record - Teratech Corp.
17 devices
Cleared
May 09, 2015
Terason uSmart3200T Ultrasound System
Radiology
68d
Cleared
Feb 20, 2015
Terason uSmart3300 Ultrasound System
Radiology
28d
Cleared
May 30, 2014
TERASON USMART3300 ULTRASOUND SYSTEM
Radiology
63d
Cleared
Apr 25, 2014
TERASON USMART3400 ULTRASOUND SYSTEM
Radiology
23d
Cleared
Mar 21, 2014
TERASON USMART3200 AND BENQ UP200ULTRASOUND SYSTEM
Radiology
17d
Cleared
May 24, 2013
TERASON USMART3200T ULTRASOUND SYSTEM
Radiology
25d
Cleared
Feb 03, 2012
TERASON T3000 ULTRASOUND SYSTEMS WITH UPDATED NEEDLE GUIDANCE GRAPHICS
Radiology
122d
Cleared
Mar 18, 2011
PROSOUND C3 / C3 CV ULTRASOUND SYSTEMS
Radiology
28d
Cleared
Jan 20, 2011
TERASON T3200 ULTRASOUND SYSTEM
Radiology
17d
Cleared
Feb 14, 2008
TERASON ECHO T/3000 ULTRASOUND SYSTEM WITH STRESS ECHO
Radiology
15d
Cleared
Jun 03, 2005
TERASON ULTRASOUND SYSTEM WITH CONTINUOUS WAVE SOPPLER
Radiology
11d
Cleared
Dec 13, 2004
TERATECH MODEL 8IOC4, 8IOL4 & 10LAP4 PROBES
Radiology
17d