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

TRACETS 2000/ELECTRODES

K Number: K863674 · Decision Mar 11, 1987
Classifications
1
FEI Numbers
191
Registration Numbers
191
Same Product Code
328
Applicant Total
27
Review Days
173

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Basic Information

Device Name
TRACETS 2000/ELECTRODES
K Number
K863674
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.2360
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Lectec Corp.
Date Received
September 19, 1986
Decision Date
March 11, 1987
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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K912450 TRACETS SME 5000
K904512 TRACET AG 4000
K893425 VITATRACE
K884108 MACROPORE MEDICAL/SURGICAL PAPER TAPE
K882216 SYNCOR (R) MODEL S-801 ECG ELECTRODE
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