Medical Device Recalls
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1 result found
510(K) Number: K883414 |
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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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Green Spec Fiberoptic Laryngoscope Handle - Stubby/Short; a battery operated fiberoptic laryngoscope... | 2 | 07/13/2006 | Teleflex Medical |
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