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

ACUITY CENTRAL STATION

K Number: K972121 · Decision Nov 7, 1997
Classifications
1
FEI Numbers
48
Registration Numbers
48
Same Product Code
13
Applicant Total
15
Review Days
155

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Basic Information

Device Name
ACUITY CENTRAL STATION
K Number
K972121
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.1025
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Protocol Systems, Inc.
Date Received
June 5, 1997
Decision Date
November 7, 1997
Product Code
MLD
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
MLD Monitor, St Segment With Alarm

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (MLD), 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
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
K910772 PROPAQ 102, 104 AND 106
Search all 15 clearances from Protocol Systems, Inc. →