Life Design Systems, Inc. - FDA 510(k) Cleared Devices
29
Total
29
Cleared
0
Denied
Life Design Systems, Inc. has 29 FDA 510(k) cleared anesthesiology devices. Based in Mchenry, US.
Historical record: 29 cleared submissions from 1982 to 1992.
Browse the complete list of FDA 510(k) cleared anesthesiology devices from this manufacturer. Filter by specialty or product code using the sidebar.
29 devices
Cleared
Dec 01, 1992
MODIFICATION MANUAL PULMON RESUSCITOR/PULMANEX(TM)
Anesthesiology
474d
Cleared
Oct 11, 1989
HUMIDI-FLEX TM
Anesthesiology
286d
Cleared
Sep 18, 1989
CHILD SIZE - FILTER FLEX (TM)
General Hospital
147d
Cleared
May 25, 1989
FLEX-CUP PERCUSSOR
Anesthesiology
37d
Cleared
May 18, 1989
PULMONARY RESUSCITATOR, MODIFICATION
Anesthesiology
49d
Cleared
Mar 20, 1989
OXYGEN CONNECTOR AND OXYGEN DELIVERY TUBING
Anesthesiology
76d
Cleared
Jan 24, 1989
MODIFIED CUSHION-FLEX(TM)
Anesthesiology
21d
Cleared
Nov 17, 1988
CUSHION FLEX(TM)
Anesthesiology
30d
Cleared
Nov 16, 1988
PULMANEX TM (NEO-NATAL SIZE)
Anesthesiology
78d
Cleared
Mar 31, 1988
HEATER WIRE BREATHING CIRCUIT
Anesthesiology
232d
Cleared
Oct 07, 1987
PULSE-OX
Anesthesiology
370d
Cleared
May 21, 1987
CARHILL ONE-WAY RESUSCITATION VALVE
Anesthesiology
170d