Blease Medical Equipment , Ltd. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Blease Medical Equipment , Ltd. has 5 FDA 510(k) cleared medical devices. Based in Appollo Beach, US.
Historical record: 5 cleared submissions from 1999 to 2004. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Blease Medical Equipment , Ltd. Filter by specialty or product code using the sidebar.
5 devices
Cleared
Oct 07, 2004
BLEASE SIRIUS ANESTHESIA SYSTEM, MODELS 3000 AND 2000
Anesthesiology
132d
Cleared
May 23, 2001
BLEASE FRONTLINE PLUS RANGE, ANESTHESIA MACHINES, MODEL 440, 560 AND 690
Anesthesiology
218d
Cleared
Aug 09, 2000
MODIFICATION TO BLEASE FRONTLINE GENIUS RANGE, ANESTHESIA MACHINES
Anesthesiology
64d
Cleared
Apr 15, 1999
BLEASE 6200 ANAESTHESIA VENTILATOR
Anesthesiology
302d
Cleared
Apr 09, 1999
BLEASE FRONTLINE GENIUS RANGE ANAESTHESIA MACHINE
Anesthesiology
296d