Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K131955 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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FullFire Diffusing Tip Laser Probe, REF: DTP101-01, DTP201-01, DTP301-01, DTP401-01, DTP501-01. Th... | 2 | 11/19/2014 | Monteris Medical Corp |
SideFire Directional Laser Probe, REF: NBP101-01, NBP201-01, NBP301-01, NBP401-01, NBP501-01. Thes... | 2 | 11/19/2014 | Monteris Medical Corp |
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