Medical Device Recalls
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1 result found
510(K) Number: K061102 |
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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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| Anesthesia Machines (digital display assembly); A gas machine for anesthesia is a device used to... | 2 | 03/26/2012 |
FEI # 3002807907 Penlon, Ltd. |
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