Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K881413 |
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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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| Weck, Electrosurgical Coagulation Suction Tube 8 (20.0cm), 11 French, with Stylet, Teleflex Medical... | 2 | 01/15/2014 |
FEI # 3005747797 Teleflex Medical |
| Weck, Electrosurgical Coagulation Suction Tube 6 (15.2cm), 11 French, with Stylet, Teleflex Medical... | 2 | 01/15/2014 |
FEI # 3005747797 Teleflex Medical |
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