Airco/Ohio Medical Products - FDA 510(k) Cleared Devices
13
Total
13
Cleared
0
Denied
Airco/Ohio Medical Products has 13 FDA 510(k) cleared anesthesiology devices. Based in Mchenry, US.
Historical record: 13 cleared submissions from 1979 to 1984.
Browse the complete list of FDA 510(k) cleared anesthesiology devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Airco/Ohio Medical Products
13 devices
Cleared
Jan 10, 1984
COAXIAL VOL. VENTILATOR CIRCUIT
Anesthesiology
97d
Cleared
Nov 29, 1983
OHIO GMS ABSORBER
Anesthesiology
67d
Cleared
Sep 12, 1983
OHIO TEMPERATURE SIMULATOR
General Hospital
52d
Cleared
Sep 01, 1983
OHIO 5400 VOLUME MONITOR
Anesthesiology
30d
Cleared
Aug 12, 1983
OHIO MODEL 922 SPIROMETER
Anesthesiology
37d
Cleared
Mar 24, 1983
OXYGEN MONITOR OHIO 5100
Anesthesiology
42d
Cleared
Sep 21, 1982
OHIO V5A ANESTHESIA VENTILATOR
Anesthesiology
36d
Cleared
Dec 31, 1981
OHIO VOLUME INCENTIVE SPIROMETER
Anesthesiology
30d
Cleared
Nov 24, 1981
OHIO NON-REUSABLE TRACHEAL TUBE MURPHY
Anesthesiology
41d
Cleared
Nov 24, 1981
OHIO NON-REUSABLE TRACHEAL TUBE MAJILL
Anesthesiology
41d
Cleared
Jun 02, 1981
DABC NONCONDUCTIVE PEDIAT. ANESTH. CIR
Anesthesiology
14d
Cleared
Mar 27, 1981
OHIO DISPOSABLE TRACHEAL TUBE
Anesthesiology
4d