FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

PAQ10 PAPER CHART RECORDER

K Number: K894607 · Decision Oct 26, 1989
Classifications
1
FEI Numbers
52
Registration Numbers
52
Same Product Code
86
Applicant Total
15
Review Days
98

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Basic Information

Device Name
PAQ10 PAPER CHART RECORDER
K Number
K894607
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
870.2810
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Protocol Systems, Inc.
Date Received
July 20, 1989
Decision Date
October 26, 1989
Product Code
DSF
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
DSF Recorder, Paper Chart

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Other Clearances by Protocol Systems, Inc.

K Number Device Name
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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. →