Spiracle Technology - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Spiracle Technology has 4 FDA 510(k) cleared medical devices. Based in Irvine, US.
Historical record: 4 cleared submissions from 1996 to 1998. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Spiracle Technology Filter by specialty or product code using the sidebar.
4 devices
Cleared
Oct 28, 1998
SPIRACLE TECHNOLOGY-BI-FLOW DEMAND/RESUSCITATOR VALVE, MODEL 504
Anesthesiology
126d
Cleared
Jul 23, 1998
TSX PRM PULMONARY RESUSCITATION MONITOR
Anesthesiology
321d
Cleared
Apr 08, 1997
SPIRACLE TECHNOLOGY - MODEL 302 OX INHALATOR
Anesthesiology
202d
Cleared
Feb 29, 1996
SPIRACLE TECHNOLOTY GASEOUS OXYGEN SUPPLY VALVE
Anesthesiology
227d