Stereotaxis Inc
6 FDA 510(k) clearances · Recalling firm
| Record | Firm | Date |
|---|---|---|
| Cronus Endovascular Guidewire, Length 210 cm (full coat), Diameter 0.014 inch, Part Number recall (Z-0590-04) | Stereotaxis Inc | 2004-07-20 |
| Cronus Endovascular Guidewire, Length 210 cm (partial coat), Diameter 0.014 inch, Part Num recall (Z-0591-04) | Stereotaxis Inc | 2004-07-20 |
| Cronus Endovascular Guidewire, Length 300 cm (partial coat), Diameter 0.014 inch, Part Num recall (Z-0592-04) | Stereotaxis Inc | 2004-07-20 |
| Floppy Cronus Endovascular Guidewire, Length 180 cm (partial coat), Diameter 0.014 inch, P recall (Z-0593-04) | Stereotaxis Inc | 2004-07-20 |
| Floppy Cronus Endovascular Guidewire, Length 300 cm (partial coat), Diameter 0.014 inch, P recall (Z-0594-04) | Stereotaxis Inc | 2004-07-20 |
| Cronus-1 Endovascular Guidewire, Length 210 cm (full coat), Diameter 0.014 inch, Part Numb recall (Z-0595-04) | Stereotaxis Inc | 2004-07-20 |
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Every clearance here is in the API, with alerts when new ones post.