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

MODEL E 600 ELECTROCARDIOGRAPH

K Number: K860767 · Decision Apr 23, 1986
Classifications
1
FEI Numbers
121
Registration Numbers
121
Same Product Code
397
Applicant Total
12
Review Days
51

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Basic Information

Device Name
MODEL E 600 ELECTROCARDIOGRAPH
K Number
K860767
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.1025
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Kone Instruments, Inc.
Date Received
March 3, 1986
Decision Date
April 23, 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 Kone Instruments, Inc.

K Number Device Name
K873345 'MICROLYTE 4/5'
K870777 PROGRESS PLUS SELECTIVE CHEMISTRY ANALYZER
K863466 M700 STRESS MONITOR
K862655 SIGNA II RESTING ECG ELECTRODE
K853354 MEDIC 4
K840200 PROGRESS SELECTIVE DHEMISTRY ANALYZ
K830433 PATIENT MONITOR 575
K830432 CENTRAL STATION 590
K822952 560
K820541 MICROLYTE
Search all 12 clearances from Kone Instruments, Inc. →