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

CARDIOSERV S

K Number: K962551 · Decision Nov 19, 1996
Classifications
1
FEI Numbers
36
Registration Numbers
36
Same Product Code
165
Applicant Total
82
Review Days
144

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Basic Information

Device Name
CARDIOSERV S
K Number
K962551
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.5300
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent - Subject to Tracking Reg.
Applicant
Marquette Electronics, Inc.
Date Received
June 28, 1996
Decision Date
November 19, 1996
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)

Similar 510(k) Clearances

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Other Clearances by Marquette Electronics, Inc.

K Number Device Name
K971868 IMPACT (INFORMING MOBILE PERSONNEL AND CARE TRACKING) PAGER SYSTEM
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
K960418 EAGLE PATIENT MONITOR
K960272 EAGLE 3000/3100 PATIENT MONITOR
K961139 EAGLE PATIENT MONITOR MODEL 3000/3100
Search all 82 clearances from Marquette Electronics, Inc. →