Flexicare Medical, Ltd. is one of 461 FDA 510(k) medical device manufacturers from United Kingdom in the dataset, ranked by real submission volume.
Flexicare Medical, Ltd. - FDA 510(k) Cleared Devices
Recent clearances: Flexicare Heated Wire Breathing Systems, DUALGUARD, O2 NASAL CANNULA WITH CO2 MONITORING
7
Total
7
Cleared
0
Denied
Flexicare Medical, Ltd. has 7 FDA 510(k) cleared medical devices. Based in Somerset, GB.
Historical record: 7 cleared submissions from 1995 to 2015. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Flexicare Medical, Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Regulatory Technology Services, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Flexicare Medical, Ltd.
7 devices
Cleared
May 15, 2015
Flexicare Heated Wire Breathing Systems
Anesthesiology
42d
Cleared
Apr 10, 2014
DUALGUARD
Anesthesiology
44d
Cleared
Mar 06, 2014
O2 NASAL CANNULA WITH CO2 MONITORING
Anesthesiology
50d
Cleared
Oct 11, 2013
CLASSIC INTERMITTENT CATHETER
Gastroenterology & Urology
51d
Cleared
Oct 06, 2009
FLEXICARE BREATHING FILTERS
General Hospital
76d
Cleared
Jun 17, 2009
FLEXICARE MEDICAL ENDOTRACHEAL TUBES
Anesthesiology
15d
Cleared
Apr 27, 1995
VENTIMASK MK IV
Anesthesiology
17d