AtriCure, Inc.
5 FDA 510(k) clearances · Recalling firm
| Record | Firm | Date |
|---|---|---|
| Cryo Module Accessories Domestic CMA-OUS, Product Catalog Number A001053 recall (Z-0927-2024) | AtriCure, Inc. | 2024-01-31 |
| Packaged, Tank Hose Assembly CMA-US, Product Catalog Number A001056 recall (Z-0928-2024) | AtriCure, Inc. | 2024-01-31 |
| Cryogenic probe for cardiac ablation surgery, packaged individually in Tyvek pouches Produ recall (Z-0895-2015) | Atricure Inc | 2014-12-30 |
| Reusable Clip Applier Manufactured by AtriCure, Inc., 6217 Centre Park Drive, West Chester recall (Z-1209-2014) | Atricure Inc | 2014-03-14 |
| Atricure Inc., Max1 Isolator Transpolar Pen. Model A000163. Used to ablate cardiac tissues recall (Z-0912-2013) | Atricure Inc | 2013-03-06 |
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Every clearance here is in the API, with alerts when new ones post.