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

INTERFERENTIAL CURRENT THERAPY UNIT

K Number: K931768 · Decision Feb 23, 1994
Classifications
1
FEI Numbers
46
Registration Numbers
46
Same Product Code
72
Applicant Total
13
Review Days
321

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Basic Information

Device Name
INTERFERENTIAL CURRENT THERAPY UNIT
K Number
K931768
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.5890
Medical Specialty
Neurology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Lumiscope Co., Inc.
Date Received
April 8, 1993
Decision Date
February 23, 1994
Product Code
LIH
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
LIH Interferential Current Therapy

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Other Clearances by Lumiscope Co., Inc.

K Number Device Name
K032714 CARDICARE MODEL MT-301F & MT-301C
K954792 LUMISCOPE MODEL 2018 THERMOMETER
K925054 INFRARED LAMP
K924081 LUMISONIC
K920099 GYMMAN
K901849 LUMISCOPE EMS 8000
K901096 LUMISCOPE ALTERNATING PRESSURE PAD & PUMP
K901726 LUMISCOPE MICRO 100
K901809 LUMISCOPE ELECTRODES MODELS EL-08,11,15,06,21,25
K894127 LUMISCOPE MODEL 1000/APCC MODEL 1000
Search all 13 clearances from Lumiscope Co., Inc. →