FDA 510(k) FDA class 2 Substantially Equivalent - Subject to Tracking Reg. 🇺🇸 United States

PROPAQ ENCORE 200 SERIES MONITOR WITH NEONATAL MODE AND IMPEDANCE PNEUMOGRAPHY OPTIONS

K Number: K951246 · Decision Feb 2, 1996
Classifications
1
FEI Numbers
3
Registration Numbers
3
Same Product Code
15
Applicant Total
15
Review Days
319

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Basic Information

Device Name
PROPAQ ENCORE 200 SERIES MONITOR WITH NEONATAL MODE AND IMPEDANCE PNEUMOGRAPHY OPTIONS
K Number
K951246
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.2377
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent - Subject to Tracking Reg.
Applicant
Protocol Systems, Inc.
Date Received
March 20, 1995
Decision Date
February 2, 1996
Product Code
FLS
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
FLS Monitor, Apnea, Facility Use

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (FLS), ordered by most recent decision date.

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Other Clearances by Protocol Systems, Inc.

K Number Device Name
K002725 MICROPAQ, MODELS 402 AND 404
K972121 ACUITY CENTRAL STATION
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
K910772 PROPAQ 102, 104 AND 106
Search all 15 clearances from Protocol Systems, Inc. →