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

CARDIO PORT 500 24-H ECG AMBULATORY MONITOR SYSTEM

K Number: K862375 · Decision Jul 1, 1986
Classifications
1
FEI Numbers
121
Registration Numbers
121
Same Product Code
397
Applicant Total
8
Review Days
7

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Basic Information

Device Name
CARDIO PORT 500 24-H ECG AMBULATORY MONITOR SYSTEM
K Number
K862375
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.1025
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Grandcor Medical Systems
Date Received
June 24, 1986
Decision Date
July 1, 1986
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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Other Clearances by Grandcor Medical Systems

K Number Device Name
K905480 SPIROSCOPE
K895547 GRANDCOR/CARDIOLINE ECT STRESS TESTING
K883410 CARDIOMEGA-T
K871890 CARDIO-MEGA SYSTEM
K864260 APPLICARD SYSTEM (ECG ELECTRODE SYSTEM)
K864978 APPLISCOPE
K864581 APPLIDYN