Medical Device Recalls
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1 result found
510(K) Number: K172356 |
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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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BladderScan Prime Plus Probe REF 0570-0395 - Product Usage: intended to be used for measuring the ur... | 2 | 12/03/2020 | Verathon, Inc. |
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