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

ECG MODULATOR

K Number: K760563 · Decision Sep 10, 1976
Classifications
1
FEI Numbers
86
Registration Numbers
86
Same Product Code
292
Applicant Total
80
Review Days
8

Basic Information

Device Name
ECG MODULATOR
K Number
K760563
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.2920
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
PHYSIO-CONTROL CORP.
Date Received
September 2, 1976
Decision Date
September 10, 1976
Product Code
DXH
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
DXH Transmitters And Receivers, Electrocardiograph, Telephone

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K Number Device Name
K991910 LIFEPAK 12 BIPHASIC
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K983393 LIFEPAK 500 BIPHASIC
K973486 LIFE PAK 12
K962359 LIFEPAK 300
K955854 LIFEPAK 500
K953204 PEDIATRIC QUIK-COMBO
K951593 LIFEPAK 11
K945511 LIFEPAK 10 DEFIBRILLATOR/MONITOR/PACEMAKER, AND LIFEPAK 11 CARDIAC MONITOR
K943301 QUIK COMBO
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