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U.S. Department of Health and Human Services

510(k) Premarket Notification
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510(k) Number K837481
Device Name BF24 DOPPLER MODEL P872 AND P874
Applicant
Medasonics, Inc.
82 Pioneer Way
P.O. Box 7268
Mountain View,  CA  94042
Correspondent
Medasonics, Inc.
82 Pioneer Way
P.O. Box 7268
Mountain View,  CA  94042
Date Received05/09/1983
Decision Date 06/24/1983
Decision Substantially Equivalent (SESE)
510k Review Panel Radiology
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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