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

RADIO TRANSPARENT ECG ELECTRODE

K Number: K761249 · Decision Dec 21, 1976
Classifications
1
FEI Numbers
191
Registration Numbers
191
Same Product Code
328
Applicant Total
83
Review Days
8

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Basic Information

Device Name
RADIO TRANSPARENT ECG ELECTRODE
K Number
K761249
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.2360
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Concept, Inc.
Date Received
December 13, 1976
Decision Date
December 21, 1976
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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