Medical Device Recalls
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1 result found
510(K) Number: K152770 |
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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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| Welch Allyn ProBP 2400 Digital Blood Pressure Device #2400, REF 901096, Rx ONLY, Made in China --- D... | 2 | 04/11/2017 | Welch Allyn Inc |
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