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

PRESSURE, LOW/HIGH MODEL C1070

K Number: K781697 · Decision Oct 27, 1978
Classifications
1
FEI Numbers
55
Registration Numbers
55
Same Product Code
77
Applicant Total
29
Review Days
17

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Basic Information

Device Name
PRESSURE, LOW/HIGH MODEL C1070
K Number
K781697
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.2600
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Applicant
Timeter Instrument Corp.
Date Received
October 10, 1978
Decision Date
October 27, 1978
Product Code
CAP
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
CAP Monitor, Airway Pressure (Includes Gauge And/Or Alarm)

Similar 510(k) Clearances

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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
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
Search all 29 clearances from Timeter Instrument Corp. →