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FDA 510(k) Applications Submitted by MEDRAD INTERVENTIONAL/POSSIS
FDA 510(k) Number
Submission Date
Device Name
Applicant
K101354
05/14/2010
FETCH 2 ASPIRATION CATHETER MODEL 109400-001
MEDRAD INTERVENTIONAL/POSSIS
K101406
05/19/2010
ANGIOJET SOLENT PROXI THROMBECTOMY SET MODEL 109676-001
MEDRAD INTERVENTIONAL/POSSIS
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