FDA 510(k) Substantially Equivalent 🇺🇸 United States

CARDIOSOFT/CARDIOSYS

K Number: K951130 · Decision Apr 4, 1996
Classifications
0
FEI Numbers
11
Registration Numbers
11
Same Product Code
82
Applicant Total
82
Review Days
388

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Basic Information

Device Name
CARDIOSOFT/CARDIOSYS
K Number
K951130
Clearance Type
Traditional
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Marquette Electronics, Inc.
Date Received
March 13, 1995
Decision Date
April 4, 1996
Product Code
LOS
Advisory Committee
Unknown
Review Advisory Committee
CV
Third Party
N

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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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