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

GEL ELECTRODE

K Number: K813176 · Decision Dec 29, 1981
Classifications
1
FEI Numbers
191
Registration Numbers
191
Same Product Code
328
Applicant Total
5
Review Days
47

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Basic Information

Device Name
GEL ELECTRODE
K Number
K813176
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.2360
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Dyn-A-Med Products
Date Received
November 12, 1981
Decision Date
December 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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K802139 SPATULA, CERVICAL CYTOLOGICAL CYTOLOGY