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

EKG (ECG) ELECTRODES

K Number: K821434 · Decision Jul 30, 1982
Classifications
1
FEI Numbers
191
Registration Numbers
191
Same Product Code
328
Applicant Total
5
Review Days
79

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Basic Information

Device Name
EKG (ECG) ELECTRODES
K Number
K821434
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.2360
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Dupaco, Inc.
Date Received
May 12, 1982
Decision Date
July 30, 1982
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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