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

NEURO PULSE

K Number: K841400 · Decision Jun 15, 1984
Classifications
1
FEI Numbers
184
Registration Numbers
184
Same Product Code
605
Applicant Total
30
Review Days
73

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Basic Information

Device Name
NEURO PULSE
K Number
K841400
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.5890
Medical Specialty
Neurology
Decision
Substantially Equivalent
Applicant
Parker Laboratories, Inc.
Date Received
April 3, 1984
Decision Date
June 15, 1984
Product Code
GZJ
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
GZJ Stimulator, Nerve, Transcutaneous, For Pain Relief

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