Devicor Medical Products Inc
3 FDA 510(k) clearances · Recalling firm
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| Record | Firm | Date |
|---|---|---|
| HydroMARK Breast Biopsy Site Marker, Model Number: 4010-02-15-T3 recall (Z-2239-2026) | Devicor Medical Products Inc | 2026-05-27 |
| Mammotome Revolve Dual Vacuum Assist Biopsy System The device is used to sample breast tis recall (Z-1512-2017) | Devicor Medical Products Inc | 2017-03-08 |
| Mammotome Revolve Dual Vacuum Assist Biopsy System Model number: MST1009 & MST0815. Each d recall (Z-2211-2016) | Devicor Medical Products Inc | 2016-07-14 |
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Every clearance here is in the API, with alerts when new ones post.