Hudson Oxygen Therapy Sales Co. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Hudson Oxygen Therapy Sales Co. - FDA 510(k) Cleared Devices
33
Total
33
Cleared
0
Denied
Hudson Oxygen Therapy Sales Co. has 33 FDA 510(k) cleared anesthesiology devices. Based in Mchenry, US.
Historical record: 33 cleared submissions from 1976 to 1990.
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 - Hudson Oxygen Therapy Sales Co.
33 devices
Cleared
Sep 04, 1990
PEEP VALVE
Anesthesiology
119d
Cleared
Jul 18, 1990
MDI ADAPTOR
Anesthesiology
148d
Cleared
May 18, 1990
IN-THE NEBULIZER
Anesthesiology
107d
Cleared
Mar 30, 1990
MANUAL RESUSCITATOR
Anesthesiology
196d
Cleared
Jan 09, 1990
INFANT C.P.A.P. MONITOR
Anesthesiology
78d
Cleared
Oct 27, 1989
CATALOG NO. 1755 1S0-NEB, A FILTERED NEBULIZER
Anesthesiology
66d
Cleared
Oct 27, 1989
VENTILARM II PORTABLE AIRWAY PRESSURE MONITOR
Anesthesiology
31d
Cleared
May 05, 1989
BACTERIA FILTER
General Hospital
121d
Cleared
May 04, 1987
NO. 1552, VALVED VENTI-COMP
Anesthesiology
60d
Cleared
Apr 21, 1987
C.P.A.P. NASAL CANNULA
Anesthesiology
28d
Cleared
Mar 06, 1987
1160 SIMPLE ISOLATION VALVE & 1161 FILTERED VALVE
Anesthesiology
52d
Cleared
Apr 02, 1984
MONITOR 5590- ANALYZER 5595EC
Anesthesiology
54d