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Angiotech Medical Device Technologies

10 FDA 510(k) clearances · PMA applicant

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RecordFirmDate
VITAGEL SURGICAL HEMOSTAT (P990030/S005)Angiotech Medical Device Technologies2004-09-13
COSEAL SURGICAL SEALANT (ORIGINAL AND PRE-MIXED) (P010022/S003)Angiotech Medical Device Technologies2003-05-06
COSEAL SURGICAL SEALANT (P010022/S002)Angiotech Medical Device Technologies2003-03-18
COSEAL SURGICAL SEALANT (PREMIXED) (P010022/S001)Angiotech Medical Device Technologies2003-02-04
COSTASIS SURGICAL HEMOSTAT (P990030/S004)Angiotech Medical Device Technologies2002-06-13
COSTASIS/DYNASTAT SURGICAL HEMOSTATS (P990030/S003)Angiotech Medical Device Technologies2002-03-14
COSTASIS/DYNASTAT SURGICAL HEMOSTAT (P990030/S002)Angiotech Medical Device Technologies2001-12-21
COSEAL SURGICAL SEALANT (COSEAL) (P010022)Angiotech Medical Device Technologies2001-12-14
COSTASIS(R)/DYNASTAT SURGICAL HEMOSTAT (P990030/S001)Angiotech Medical Device Technologies2001-01-02
VITAGEL SURGICAL HEMOSTAT (P990030)Angiotech Medical Device Technologies2000-06-13

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Every clearance here is in the API, with alerts when new ones post.