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

MARQUETTE SERIES 360 DEFIBRILLATOR

K Number: K921487 · Decision Dec 29, 1992
Classifications
1
FEI Numbers
36
Registration Numbers
36
Same Product Code
165
Applicant Total
82
Review Days
274

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Basic Information

Device Name
MARQUETTE SERIES 360 DEFIBRILLATOR
K Number
K921487
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.5300
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Marquette Electronics, Inc.
Date Received
March 30, 1992
Decision Date
December 29, 1992
Product Code
LDD
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
LDD Dc-Defibrillator, Low-Energy, (Including Paddles)

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Other Clearances by Marquette Electronics, Inc.

K Number Device Name
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K971683 WIRELESS LAN (LOCAL AREA NETWORK) - WIRELESS ETHERNET
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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