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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Plethysmograph, Impedance
510(k) Number K893963
Device Name VERIPOID 50 BIO-ELECTRICAL IMPEDANCE METER
Applicant
V.S.B.B. Technologies, Inc.
P.O. Box 9072
Portland,  OR  97207
Applicant Contact WILLIAM WEINSTEIN
Correspondent
V.S.B.B. Technologies, Inc.
P.O. Box 9072
Portland,  OR  97207
Correspondent Contact WILLIAM WEINSTEIN
Regulation Number870.2770
Classification Product Code
DSB  
Date Received06/02/1989
Decision Date 09/05/1989
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Cardiovascular
510k Review Panel Cardiovascular
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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