FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

CRITERION I

K Number: K834274 · Decision Apr 13, 1984
Classifications
1
FEI Numbers
83
Registration Numbers
83
Same Product Code
286
Applicant Total
29
Review Days
127

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Basic Information

Device Name
CRITERION I
K Number
K834274
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.5440
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Applicant
Timeter Instrument Corp.
Date Received
December 8, 1983
Decision Date
April 13, 1984
Product Code
CAW
Advisory Committee
Anesthesiology
Review Advisory Committee
AN
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
CAW Generator, Oxygen, Portable

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Other Clearances by Timeter Instrument Corp.

K Number Device Name
K875075 RT-200 COMPUTER INTERFACE
K875074 VACUMATE INTERMITTENT/CONTINUOUS CONTROLLER,VM2000
K871603 CRITERION II & IIA OXYGEN CONCENTRATORS
K864836 L.A.P. SPIROMETER
K823775 BORDON GAGE REGULATOR #BG
K822746 RT-200 CALIBRATION ANALYZER
K812766 PCS-5 ACCESSORIES
K813235 DISS FEMALE AIR ADAPTOR
K813234 OHIO AIR ADAPTOR
K812767 SNIFF AIR COMPRESSOR #SF-6
Search all 29 clearances from Timeter Instrument Corp. →