Remote Diagnostic Technologies , Ltd. is one of 462 FDA 510(k) medical device manufacturers from United Kingdom in the dataset, ranked by real submission volume.
Remote Diagnostic Technologies , Ltd. - FDA 510(k) Cleared Devices
Recent clearances: Tempus Pro Patient Monitor, Tempus Pro Patient Monitor, TEMPUS PRO WITH ENHANCED FEATURES
11
Total
11
Cleared
0
Denied
Remote Diagnostic Technologies , Ltd. has 11 FDA 510(k) cleared cardiovascular devices. Based in Basingstoke, Hampshire, GB.
Historical record: 11 cleared submissions from 2001 to 2018.
Browse the complete list of FDA 510(k) cleared cardiovascular devices from this manufacturer. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Intertek Testing Services, N.V. Kema and Regulatory Technology Services, LLC.
FDA 510(k) Regulatory Record - Remote Diagnostic Technologies , Ltd.
11 devices
Cleared
Jan 10, 2018
Tempus Pro Patient Monitor
Cardiovascular
30d
Cleared
Jul 06, 2017
Tempus Pro Patient Monitor
Cardiovascular
129d
Cleared
Aug 14, 2014
TEMPUS PRO WITH ENHANCED FEATURES
Cardiovascular
231d
Cleared
Aug 12, 2014
TEMPUS PRO ACCESSORIES (ULTRASOUND & VIDEO LARYNGOSCOPE PROBE)
Cardiovascular
225d
Cleared
May 16, 2014
TEMPUS PRO EXTENDED FEATURES
Cardiovascular
141d
Cleared
Jun 05, 2013
TEMPUS PRO PATIENT MONITOR
Cardiovascular
77d
Cleared
Dec 15, 2011
TEMPUSIC PATIENT MONITOR
Cardiovascular
56d
Cleared
May 11, 2010
TEMPUS IC PROFESSIONAL PATIENT MONITOR
Cardiovascular
6d
Cleared
Oct 10, 2008
TEMPUSIC PATIENT MONITOR
Cardiovascular
23d
Cleared
Mar 05, 2004
TEMPUS 2000 PATIENT MONITOR, MODEL 00-0002
Cardiovascular
130d
Cleared
May 14, 2001
TEMPUS 2000 PATIENT MONITOR, MODEL 00-0001
Cardiovascular
90d