Angiodynamics Inc. (Navilyst Medical Inc.)
4 FDA 510(k) clearances · Recalling firm
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| Record | Firm | Date |
|---|---|---|
| NAMIC Fluid Delivery Set - 72" (183cm) UPN H965913000051, Catalog 91300005 recall (Z-1853-2017) | Angiodynamics Inc. (Navilyst Medical Inc.) | 2017-03-29 |
| Celerity ECG Cable Accessory Pack, STERILE, Rx ONLY - distributed under the following labe recall (Z-1137-2017) | Angiodynamics Inc. (Navilyst Medical Inc.) | 2017-02-03 |
| Vortex MEDICAL AngioVac Circuit, REF/UPN VTX3100, STERILE, Rx Only, Single Use Only -- The recall (Z-1701-2016) | Angiodynamics Inc. (Navilyst Medical Inc.) | 2016-05-20 |
| AngioVac Circuit Pack (Tandem Packs), REF/Catalog No. 25-187, UPN H965251870, STERILE, Rx recall (Z-1702-2016) | Angiodynamics Inc. (Navilyst Medical Inc.) | 2016-05-20 |
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Every clearance here is in the API, with alerts when new ones post.