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

ADVANCED MEDICAL PRODUCTS DR PULSE (TENS)

K Number: K852837 · Decision Aug 28, 1985
Classifications
1
FEI Numbers
184
Registration Numbers
184
Same Product Code
605
Applicant Total
14
Review Days
57

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Basic Information

Device Name
ADVANCED MEDICAL PRODUCTS DR PULSE (TENS)
K Number
K852837
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.5890
Medical Specialty
Neurology
Decision
Substantially Equivalent
Applicant
Advanced Medical Products, Inc.
Date Received
July 2, 1985
Decision Date
August 28, 1985
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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