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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Stimulator, Muscle, Powered
510(k) Number K844727
Device Name MODEL 1000
Applicant
Verite
1614 W. Anaheim Rd.
Harbor City,  CA  90710
Applicant Contact DE LANGIS
Correspondent
Verite
1614 W. Anaheim Rd.
Harbor City,  CA  90710
Correspondent Contact DE LANGIS
Regulation Number890.5850
Classification Product Code
IPF  
Date Received12/04/1984
Decision Date 07/09/1985
Decision SUBSTANTIALLY EQUIVALENT FOR SOME INDICATIONS (SN)
Regulation Medical Specialty Physical Medicine
510k Review Panel Physical Medicine
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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