Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K040917 |
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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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| Philips M1026B IntelliVue Anesthesia Gas Modules with manifolds | 2 | 08/24/2010 |
FEI # 1218950 Philips Healthcare Inc. |
| Philips M1026BT Gas Modules with manifolds | 2 | 08/24/2010 |
FEI # 1218950 Philips Healthcare Inc. |
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