Angiotech
Angiotech holds FDA 510(k) medical device clearances, first cleared 2007, most recent 2015.
Top product codes for Angiotech
Recent clearances by Angiotech
- K151112 — Quill Polypropylene Knotless Tissue-Closure Device, Variable Loop Design
- DEN090007 — BIO-SEAL LUNG BIOPSY TRACT SYSTEM
- K120827 — QUILL PDO KNOTLESS TISSUE-CLOSURE DEVICE (POLYDIXANONE)
- K113744 — QUILL PDO KNOTLESS TISSUE-CLOSURE DEVICE (POLYDIOXANONE)
- K113800 — QUILL QUADRAHELIX TISSUE-CLOSURE DEVICE
- K073672 — SKATER BILIARY CATHETER
- K070610 — SKATER BILIARY CATHETER
Data sourced from openFDA. This site is unofficial and independent of the FDA.