Medical Device Manufacturer · US , Mchenry , IL

Timeter Instrument Corp. - FDA 510(k) Cleared Devices

29 submissions · 29 cleared · Since 1976

Total

Cleared

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.

Timeter Instrument Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Timeter Instrument Corp.

29 devices

1-12 of 29

Cleared Apr 21, 1988

RT-200 COMPUTER INTERFACE

K875075 · BXX

Anesthesiology · 134d

Cleared Feb 22, 1988

VACUMATE INTERMITTENT/CONTINUOUS CONTROLLER,VM2000

K875074 · KDP

General Hospital · 75d

Cleared Aug 13, 1987

CRITERION II & IIA OXYGEN CONCENTRATORS

K871603 · CAW

Anesthesiology · 111d

Anesthesiology · 127d

Cleared Jan 14, 1983

BORDON GAGE REGULATOR #BG

K823775 · CCN

Anesthesiology · 31d

Cleared Oct 13, 1982

RT-200 CALIBRATION ANALYZER

DISS FEMALE AIR ADAPTOR

K813235 · BYK

Anesthesiology · 21d

Cleared Nov 27, 1981

SNIFF AIR COMPRESSOR #SF-6

Timeter Instrument Corp. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Timeter Instrument Corp.

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