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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name interferential current therapy
510(k) Number K952683
Device Name APEX MEDICAL CORP. PORTABLE INTERFERENTIAL STIMULATION DEVICE
Applicant
WHOLESALE MEDICAL IMPORTS, INC.
55 NORTHERN BLVD.
SUITE 410
GREAT NECK,  NY  11021
Applicant Contact SUSAN D GOLDSTEIN-FALK
Correspondent
WHOLESALE MEDICAL IMPORTS, INC.
55 NORTHERN BLVD.
SUITE 410
GREAT NECK,  NY  11021
Correspondent Contact SUSAN D GOLDSTEIN-FALK
Regulation Number882.5890
Classification Product Code
LIH  
Date Received06/12/1995
Decision Date 04/01/1997
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Neurology
510k Review Panel Neurology
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
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