Angiotech
Vancouver, Bc, CA
Angiotech appears in FDA device records in Vancouver, Bc, CA. FDA records list 7 510(k) clearances between and , no PMA records and no registered establishments. As of , FDA records show no recalls for this company.
FDA records held for this company
- 510(k) clearances
- 7
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 7 510(k) clearances for Angiotech between 2007 and 2015. The busiest year on record is 2012, with 4. The most recent is 2015, with 1.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 2007 | 1 |
| 2008 | 1 |
| 2012 | 4 |
| 2015 | 1 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K151112 | Quill Polypropylene Knotless Tissue-Closure Device, Variable Loop Design | GAW | Substantially Equivalent | |
| DEN090007 | BIO-SEAL LUNG BIOPSY TRACT SYSTEM | OMT | Unknown | |
| K120827 | QUILL PDO KNOTLESS TISSUE-CLOSURE DEVICE (POLYDIXANONE) | NEW | Substantially Equivalent | |
| K113744 | QUILL PDO KNOTLESS TISSUE-CLOSURE DEVICE (POLYDIOXANONE) | NEW | Substantially Equivalent | |
| K113800 | QUILL QUADRAHELIX TISSUE-CLOSURE DEVICE | GAW | Substantially Equivalent | |
| K073672 | SKATER BILIARY CATHETER | FGE | Substantially Equivalent | |
| K070610 | SKATER BILIARY CATHETER | FGE | Substantially Equivalent |
Registered establishments
No FDA establishment registrations recorded against this company.
FDA product codes
Recall records
No recall records for this company in the ingested FDA data.
Verification record
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Data as of , FDA export datePage updated Source: openFDA, public domain