Todd Industries, Inc. - FDA 510(k) Cleared Devices
11
Total
11
Cleared
0
Denied
Todd Industries, Inc. has 11 FDA 510(k) cleared anesthesiology devices. Based in Mchenry, US.
Historical record: 11 cleared submissions from 1981 to 1981.
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 - Todd Industries, Inc.
11 devices
Cleared
Mar 17, 1981
NOSECLIP #6118
Anesthesiology
36d
Cleared
Mar 17, 1981
ADULT MASKS & PEDIATRIC MASKS
Anesthesiology
35d
Cleared
Mar 17, 1981
LIFELINE IPPB SET-UP
Anesthesiology
35d
Cleared
Mar 17, 1981
NASAL CANNULA
Anesthesiology
35d
Cleared
Mar 17, 1981
NEBULIZERS
Anesthesiology
35d
Cleared
Mar 17, 1981
OXYGEN TUBING
Anesthesiology
35d
Cleared
Mar 17, 1981
CONNECTOR ADAPTERS
Anesthesiology
34d
Cleared
Mar 17, 1981
CORRUGATED FLEX TUBING
Anesthesiology
34d
Cleared
Mar 17, 1981
VENTURI MASK/DELIVERY SYSTEM #'S
Anesthesiology
33d
Cleared
Mar 13, 1981
CORRUGATED FLEX TUBING #6000,
Anesthesiology
29d
Cleared
Mar 13, 1981
VENTURI MASK/DELIVERY SYSTEM #6078
Anesthesiology
22d