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

PROPAQ 102, 104 AND 106

K Number: K910772 · Decision Apr 12, 1991
Classifications
1
FEI Numbers
428
Registration Numbers
428
Same Product Code
1216
Applicant Total
15
Review Days
49

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Basic Information

Device Name
PROPAQ 102, 104 AND 106
K Number
K910772
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.1130
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Protocol Systems, Inc.
Date Received
February 22, 1991
Decision Date
April 12, 1991
Product Code
DXN
Advisory Committee
Cardiovascular
Review Advisory Committee
CV
Third Party
N

Classifications

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

Product Code Device Name
DXN System, Measurement, Blood-Pressure, Non-Invasive

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Other Clearances by Protocol Systems, Inc.

K Number Device Name
K002725 MICROPAQ, MODELS 402 AND 404
K972121 ACUITY CENTRAL STATION
K951246 PROPAQ ENCORE 200 SERIES MONITOR WITH NEONATAL MODE AND IMPEDANCE PNEUMOGRAPHY OPTIONS
K945071 PROPAQ 200 MONITOR
K935846 MODEL ACUITY CENTRAL STATION
K934711 PROPAQ ECG TELEMETRY OPTION
K921497 PROPAQ MONITORS, MODIFICATION
K914838 PROPAQ 102,104,106,102EL,104EL,&106EL
K913193 MODEL 100 CENTRAL STATION
K910882 PROPAQ 102EL, 104EL AND 106EL
Search all 15 clearances from Protocol Systems, Inc. →