Celsion Corporation
2 FDA 510(k) clearances · Recalling firm
| Record | Firm | Date |
|---|---|---|
| Prolieve Thermodilatation Kit, consisting of a Prolieve Thermodilatation Catheter, Proliev recall (Z-1248-06) | Celsion Corporation | 2006-07-19 |
| Prolieve Thermodilatation System, model number M0068808000, labeled in part***Distributed recall (Z-1339-04) | Celsion Corporation | 2004-08-11 |
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Every clearance here is in the API, with alerts when new ones post.