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

TENS GB1001 DEVICE

K Number: K850855 · Decision Jan 9, 1986
Classifications
1
FEI Numbers
184
Registration Numbers
184
Same Product Code
605
Applicant Total
14
Review Days
314

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Basic Information

Device Name
TENS GB1001 DEVICE
K Number
K850855
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.5890
Medical Specialty
Neurology
Decision
Substantially Equivalent
Applicant
Medicon, Inc.
Date Received
March 1, 1985
Decision Date
January 9, 1986
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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