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

INTERCEPT T.E.N.S. DEVICE

K Number: K880492 · Decision Apr 18, 1988
Classifications
1
FEI Numbers
184
Registration Numbers
184
Same Product Code
605
Applicant Total
10
Review Days
74

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Basic Information

Device Name
INTERCEPT T.E.N.S. DEVICE
K Number
K880492
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.5890
Medical Specialty
Neurology
Decision
Substantially Equivalent
Applicant
Medical Design & Manufacturing Corp.
Date Received
February 4, 1988
Decision Date
April 18, 1988
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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K902822 MEDICAL DESIGNS, INC., SPECTRUM II TENS DEVICE
K895604 SOFT-EZ REUSABLE SELF-ADHERING PIGTAIL ELECTRODES
K834138 HYPO SUTURE
K821848 ASSURE-MALE EXTERNAL INCONTINCE CATHETER
K811224 MINISTIM
K810222 LIMB ORHTOSIS