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FDA 510(k) Applications Submitted by ROBERT PELIKS
FDA 510(k) Number
Submission Date
Device Name
Applicant
K120440
02/13/2012
PRESTO BREAST BIOPSY DEVICE
SONTINA MEDICAL, LLC
K133702
12/03/2013
PRESTO BREAST BIOPSY DEVICE
SONTINA MEDICAL, LLC
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