Timeter Instrument Corp. - FDA 510(k) Cleared Devices
29
Total
29
Cleared
0
Denied
Timeter Instrument Corp. has 29 FDA 510(k) cleared anesthesiology devices. Based in Mchenry, US.
Historical record: 29 cleared submissions from 1976 to 1988.
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
Apr 21, 1988
RT-200 COMPUTER INTERFACE
Anesthesiology
134d
Cleared
Feb 22, 1988
VACUMATE INTERMITTENT/CONTINUOUS CONTROLLER,VM2000
General Hospital
75d
Cleared
Aug 13, 1987
CRITERION II & IIA OXYGEN CONCENTRATORS
Anesthesiology
111d
Cleared
Mar 06, 1987
L.A.P. SPIROMETER
Anesthesiology
87d
Cleared
Apr 13, 1984
CRITERION I
Anesthesiology
127d
Cleared
Jan 14, 1983
BORDON GAGE REGULATOR #BG
Anesthesiology
31d
Cleared
Oct 13, 1982
RT-200 CALIBRATION ANALYZER
Anesthesiology
33d
Cleared
Dec 17, 1981
PCS-5 ACCESSORIES
Anesthesiology
73d
Cleared
Dec 08, 1981
OHIO AIR ADAPTOR
Anesthesiology
21d
Cleared
Dec 08, 1981
DISS FEMALE AIR ADAPTOR
Anesthesiology
21d
Cleared
Nov 27, 1981
SNIFF AIR COMPRESSOR #SF-6
Anesthesiology
53d
Cleared
Nov 16, 1981
DATASCRIBE #DS-40
Anesthesiology
42d