Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K060541 |
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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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Philips M1019A IntelliVue G5 Anesthesia Gas Modules with manifolds | 2 | 08/24/2010 | Philips Healthcare Inc. |
Philips M1013A IntelliVue G1 Anesthesia Gas Modules with manifolds | 2 | 08/24/2010 | Philips Healthcare Inc. |
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