FDA 510(k) Applications Submitted by ANGIOLOGICA B. M. SRL
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K043191 | 11/17/2004 | REPOL ANGIMESH, ANGIMESH PRE, FOLDED MESH, REPOL PLUG BASIC, REPOL PLUG CAP, REPOL PLUG FLOWER AND WINGS MESH | ANGIOLOGICA B. M. SRL |
| K090432 | 02/19/2009 | HEMORPEX SYSTEM | ANGIOLOGICA B. M. SRL |
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