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

ADULT ECG ELECTRODE #60-0724

K Number: K810103 · Decision Jan 29, 1981
Classifications
1
FEI Numbers
191
Registration Numbers
191
Same Product Code
328
Applicant Total
55
Review Days
13

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Basic Information

Device Name
ADULT ECG ELECTRODE #60-0724
K Number
K810103
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.2360
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Aspen Laboratories, Inc.
Date Received
January 16, 1981
Decision Date
January 29, 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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