Medical Device Recalls
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1 result found
510(K) Number: K112998 |
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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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AutoPulse Li-ion Battery used on the AutoPulse Resuscitation System Model 100. used as an adjunct t... | 2 | 10/21/2022 | ZOLL Circulation, Inc. |
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