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

RESUBMITTED STANDARD MICROPORE ECG ELECTRODE

K Number: K874628 · Decision Dec 7, 1987
Classifications
1
FEI Numbers
191
Registration Numbers
191
Same Product Code
328
Applicant Total
26
Review Days
46

Basic Information

Device Name
RESUBMITTED STANDARD MICROPORE ECG ELECTRODE
K Number
K874628
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.2360
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
LABELTAPE MEDITECT, INC.
Date Received
October 22, 1987
Decision Date
December 7, 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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