Angiotech Medical Device Technologies
10 FDA 510(k) clearances · PMA applicant
◉ Watch Angiotech Medical Device Technologies
| Record | Firm | Date |
|---|---|---|
| VITAGEL SURGICAL HEMOSTAT (P990030/S005) | Angiotech Medical Device Technologies | 2004-09-13 |
| COSEAL SURGICAL SEALANT (ORIGINAL AND PRE-MIXED) (P010022/S003) | Angiotech Medical Device Technologies | 2003-05-06 |
| COSEAL SURGICAL SEALANT (P010022/S002) | Angiotech Medical Device Technologies | 2003-03-18 |
| COSEAL SURGICAL SEALANT (PREMIXED) (P010022/S001) | Angiotech Medical Device Technologies | 2003-02-04 |
| COSTASIS SURGICAL HEMOSTAT (P990030/S004) | Angiotech Medical Device Technologies | 2002-06-13 |
| COSTASIS/DYNASTAT SURGICAL HEMOSTATS (P990030/S003) | Angiotech Medical Device Technologies | 2002-03-14 |
| COSTASIS/DYNASTAT SURGICAL HEMOSTAT (P990030/S002) | Angiotech Medical Device Technologies | 2001-12-21 |
| COSEAL SURGICAL SEALANT (COSEAL) (P010022) | Angiotech Medical Device Technologies | 2001-12-14 |
| COSTASIS(R)/DYNASTAT SURGICAL HEMOSTAT (P990030/S001) | Angiotech Medical Device Technologies | 2001-01-02 |
| VITAGEL SURGICAL HEMOSTAT (P990030) | Angiotech Medical Device Technologies | 2000-06-13 |
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Every clearance here is in the API, with alerts when new ones post.