FDA 510(k) Applications Submitted by KERRIE HAMBLIN

FDA 510(k) Number Submission Date Device Name Applicant
K142443 09/02/2014 Site-Rite 6 Ultrasound System with Pinpoint GT Technology C.R. Bard, Inc
K152554 09/08/2015 Site-Rite 8 Ultrasound System, Site-Rite 8 Ultrasound System with Pinpoint GT Technology C.R. Bard, Inc.
K132942 09/19/2013 SITE-RITE VISION II ULTRASOUND SYSTEM C.R. BARD, INC.


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