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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 K921441
Device Name INTERFERENTIAL STIMULATOR MODEL INF 4150/A
Applicant
Biomedical Life Systems, Inc.
1120 Sycamore Ave., Suite F
P.O. Box 1360
Vista,  CA  92083
Applicant Contact RICHARD SAXON
Correspondent
Biomedical Life Systems, Inc.
1120 Sycamore Ave., Suite F
P.O. Box 1360
Vista,  CA  92083
Correspondent Contact RICHARD SAXON
Regulation Number882.5890
Classification Product Code
LIH  
Date Received03/25/1992
Decision Date 05/08/1992
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Neurology
510k Review Panel Neurology
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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