Medical Device Recalls
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1 result found
510(K) Number: K221700 |
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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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| Brand Name: AutoPulse NXT Resuscitation System Product Name: AutoPulse NXT Platform Model/Catalog ... | 1 | 04/11/2025 |
FEI # 3003793491 ZOLL Circulation, Inc. |
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