Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K033089 |
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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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MODEL P8400 HANDLE WITH INTEGRATED CABLE, FOR USE WITH MODEL P8400 CONTROLLER, REF 7013-8050, QTY (1... | 2 | 09/28/2010 | Hemostatix Medical Technologies LLC |
HEMOSTATIX HANDLE, FOR USE WITH MODELS 150 AND 600D HEMOSTATIX CONTROLLERS, REF 7013-5050, QTY (1), ... | 2 | 09/28/2010 | Hemostatix Medical Technologies LLC |
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