Medical Device Recalls
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1 result found
510(K) Number: K914514 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Electrohydraulic lithotripter probe, 1.9 FR 375 cm, Model 9-195-371DS used with a Model 9-201-00 Aut... | 2 | 11/08/2017 | Northgate Technologies, Inc. |
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