Inhalation Plastics - FDA 510(k) Cleared Devices
7
Total
7
Cleared
0
Denied
Inhalation Plastics has 7 FDA 510(k) cleared medical devices. Based in Chicago, US.
Historical record: 7 cleared submissions from 1988 to 1995. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Inhalation Plastics Filter by specialty or product code using the sidebar.
7 devices
Cleared
Jan 13, 1995
SPIRO-FLEX
Anesthesiology
119d
Cleared
Apr 15, 1992
THERMO-FLOW SET
Anesthesiology
180d
Cleared
Sep 10, 1990
AEROMIST II NEBULIZER
Anesthesiology
173d
Cleared
Apr 19, 1990
FILT-R-ALL BACTERIAL/VIRAL FILTER
General Hospital
48d
Cleared
Mar 15, 1990
ANESTHESIA BREATHING CIRCUIT
Anesthesiology
36d
Cleared
Jan 22, 1990
FILT-R-ALL BACTERIAL FILTER
General Hospital
48d
Cleared
Feb 02, 1988
STERILIZATION OF DEVICES BY RADIATION
Anesthesiology
105d