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

SIGNA II RESTING ECG ELECTRODE

K Number: K862655 · Decision Aug 6, 1986
Classifications
1
FEI Numbers
191
Registration Numbers
191
Same Product Code
328
Applicant Total
12
Review Days
23

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Basic Information

Device Name
SIGNA II RESTING ECG ELECTRODE
K Number
K862655
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.2360
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Kone Instruments, Inc.
Date Received
July 14, 1986
Decision Date
August 6, 1986
Product Code
DRX
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
DRX Electrode, Electrocardiograph

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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
K860767 MODEL E 600 ELECTROCARDIOGRAPH
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. →