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

TRAM PATIENT MONITOR

K Number: K900540 · Decision Jul 17, 1990
Classifications
1
FEI Numbers
121
Registration Numbers
121
Same Product Code
397
Applicant Total
82
Review Days
162

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Basic Information

Device Name
TRAM PATIENT MONITOR
K Number
K900540
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.1025
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Marquette Electronics, Inc.
Date Received
February 5, 1990
Decision Date
July 17, 1990
Product Code
DSI
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
DSI Detector And Alarm, Arrhythmia

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K972199 SIGNAL-AVERAGED HIGH RESOLUTION P WAVE ANALYSIS
K962547 CARDIOSERV P
K963120 RESPONDER 2500 DEFIBRILLATOR AND CARDIAC CARE SYSTEM
K962827 ALARM DISPLAY UNIT/PAGER-LAN SYSTEM (ADU)
K964750 EAGLE 4000 PATIENT MONITOR
K962551 CARDIOSERV S
K960418 EAGLE PATIENT MONITOR
K960272 EAGLE 3000/3100 PATIENT MONITOR
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