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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