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

VACUMATE INTERMITTENT/CONTINUOUS CONTROLLER,VM2000

K Number: K875074 · Decision Feb 22, 1988
Classifications
1
FEI Numbers
29
Registration Numbers
29
Same Product Code
20
Applicant Total
29
Review Days
75

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Basic Information

Device Name
VACUMATE INTERMITTENT/CONTINUOUS CONTROLLER,VM2000
K Number
K875074
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.6740
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
Timeter Instrument Corp.
Date Received
December 9, 1987
Decision Date
February 22, 1988
Product Code
KDP
Advisory Committee
General Hospital
Review Advisory Committee
HO
Third Party
N

Classifications

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

Product Code Device Name
KDP Regulator, Vacuum

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Other Clearances by Timeter Instrument Corp.

K Number Device Name
K875075 RT-200 COMPUTER INTERFACE
K871603 CRITERION II & IIA OXYGEN CONCENTRATORS
K864836 L.A.P. SPIROMETER
K834274 CRITERION I
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. →