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

TENSAGAIN

K Number: K872574 · Decision Jul 23, 1987
Classifications
1
FEI Numbers
243
Registration Numbers
243
Same Product Code
436
Applicant Total
20
Review Days
23

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Basic Information

Device Name
TENSAGAIN
K Number
K872574
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.1320
Medical Specialty
Neurology
Decision
Substantially Equivalent
Applicant
Ferris Mfg. Corp.
Date Received
June 30, 1987
Decision Date
July 23, 1987
Product Code
GXY
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
GXY Electrode, Cutaneous

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K982306 POLYTUBE
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