Monteris Medical Corp
4 FDA 510(k) clearances · Recalling firm
| Record | Firm | Date |
|---|---|---|
| MONTERIS MEDICAL NEUROBLATE SYSTEM, used for MRI-guided neurosurgical ablation. recall (Z-0194-2018) | Monteris Medical Corp | 2018-03-20 |
| NeuroBlate System SideFire Select 2.2 mm Directional Laser Probe, Sterile EO. Model #s SFS recall (Z-1614-2016) | Monteris Medical Corp | 2016-05-16 |
| SideFire Directional Laser Probe, REF: NBP101-01, NBP201-01, NBP301-01, NBP401-01, NBP501- recall (Z-0227-2015) | Monteris Medical Corp | 2014-11-19 |
| FullFire Diffusing Tip Laser Probe, REF: DTP101-01, DTP201-01, DTP301-01, DTP401-01, DTP50 recall (Z-0228-2015) | Monteris Medical Corp | 2014-11-19 |
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Every clearance here is in the API, with alerts when new ones post.