Medical Device Recalls
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1 result found
510(K) Number: K992545 |
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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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TM-300 Traction System; an Rx software driven device used for patient traction; Manufactured for Sam... | 3 | 08/31/2005 | Sammons Preston Rolyan, An Ability One Company |
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