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

CADWELL 8400

K Number: K830771 · Decision Apr 12, 1983
Classifications
1
FEI Numbers
89
Registration Numbers
89
Same Product Code
137
Applicant Total
46
Review Days
32

Basic Information

Device Name
CADWELL 8400
K Number
K830771
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.1870
Medical Specialty
Neurology
Decision
Substantially Equivalent
Applicant
CADWELL LABORATORIES, INC.
Date Received
March 11, 1983
Decision Date
April 12, 1983
Product Code
GWF
Advisory Committee
Neurology
Review Advisory Committee
NE
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
GWF Stimulator, Electrical, Evoked Response

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