Medical Device Recalls
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1 result found
510(K) Number: K101680 |
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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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ProBP 3400 Digital Blood Pressure Device ((handheld, desk mount, wall mount models) Model: 34X... | 2 | 05/21/2021 | Welch Allyn Inc |
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