Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K811742 |
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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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ECMO Heater Model 333W, Cardiopulmonary bypass temperature controllers. This device is intended ... | 2 | 07/01/2011 | Cincinnati Sub-Zero Products Inc |
ECMO Heater Model 333, Cardiopulmonary bypass temperature controller. This device is intended to... | 2 | 07/01/2011 | Cincinnati Sub-Zero Products Inc |
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