Medical Device Recalls
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1 result found
510(K) Number: K152317 |
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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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Mederi Stretta Catheter and Accessory Kit, Sterile For Use with the MEDERI MDRF1 GENERATOR ONLY. ... | 2 | 05/08/2017 | Mederi Therapeutics, Inc |
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