FDA 510(k), K974393, VASO PRESS SYSTEM

FDA 510(k), K974393, VASO PRESS SYSTEM

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510(K) Number: K974393
Device Name: VASO PRESS SYSTEM
Manufacturer: BRITT CORP., INC.
Device Classification Name: sleeve, limb, compressible
Regulation Number: 870.5800
Classification Product Code: JOW
Date Received: 11/21/1997
Decision Date: 03/19/1999
Regulation Medical Specialty: Cardiovascular
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