Medical Device Recalls
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1 result found
510(K) Number: K160685 |
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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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S4 and patient cable for the S4 Wireless Telemeter with the following device names: CABLE 10 WIRE LF... | 2 | 04/29/2020 | WELCH ALLYN, INC/MORTARA |
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