Medical Device Recalls
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1 to 4 of 4 Results
510(K) Number: K160648 |
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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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Medtronic MiniMed(TM) Mio(TM) (MMT-921, 921T, 923, 923T, 925, 925T, 941, 941T, 943, 943T, 945, 945T,... | 2 | 11/18/2017 | Medtronic Inc. |
Medtronic MiniMed(TM) Quick-set(TM) (MMT-394, 394T, 399, 399T, 387, 387T, 398, 398T, 397, 397T, 386,... | 2 | 11/18/2017 | Medtronic Inc. |
Medtronic MiniMed(TM) Silhouette(TM) (MMT-377, 377T, 378, 378T, 384, 384T, 368, 368T, 381, 381T, 382... | 2 | 11/18/2017 | Medtronic Inc. |
Medtronic MiniMed(TM) Sure-T(TM) (MMT-862, 862T, 864, 864T, 866, 866T, 874, 874T, 876, 876T, 884, 88... | 2 | 11/18/2017 | Medtronic Inc. |
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