Medical Device Recalls
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1 result found
510(K) Number: K062523 |
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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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Conditional Fiber Optic Laryngoscope Kit, which contains laryngoscope blades, handles and 2 battery ... | 2 | 05/02/2007 | Teleflex Medical |
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