Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K040862 |
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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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NeoPAP Neonatal CPAP/Humidification System (Ventilator, Continuous). Model number 1025310 | 2 | 07/01/2006 | Respironics, Inc. |
NeoPAP Neonatal CPAP/Humidification System (Ventilator, Continuous) | 2 | 04/07/2006 | Respironics, Inc. |
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