Medical Device Recalls
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1 result found
510(K) Number: K191597 |
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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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Stealth Autoguide Tracker, Model: 28248, which is an instrument in the Stealth Autoguide Basic Instr... | 2 | 12/22/2021 | Medtronic Navigation, Inc. |
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