Medical Device Recalls
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1 result found
510(K) Number: K970277 |
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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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Liquid Waste Bottle, Catalog#10291587. The Immulite 2000 systems are continuous random-access ins... | 2 | 05/23/2015 | Siemens Medical Solutions Diagnostics |
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