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

THE NEW 1600 ELECTRODE

K Number: K812878 · Decision Nov 2, 1981
Classifications
1
FEI Numbers
191
Registration Numbers
191
Same Product Code
328
Applicant Total
21
Review Days
19

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Basic Information

Device Name
THE NEW 1600 ELECTRODE
K Number
K812878
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.2360
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Andover Medical, Inc.
Date Received
October 14, 1981
Decision Date
November 2, 1981
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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K860283 AMI CARDIO-PAD
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