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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 K931768
Device Name INTERFERENTIAL CURRENT THERAPY UNIT
Applicant
LUMISCOPE CO., INC.
400 RARITAN CENTER PKWY.
EDISON,  NJ  08837
Applicant Contact STEPHEN WHITTENBURG
Correspondent
LUMISCOPE CO., INC.
400 RARITAN CENTER PKWY.
EDISON,  NJ  08837
Correspondent Contact STEPHEN WHITTENBURG
Regulation Number882.5890
Classification Product Code
LIH  
Date Received04/08/1993
Decision Date 02/23/1994
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Neurology
510k Review Panel Neurology
Type Traditional
Reviewed by Third Party No
Combination Product No
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