Medical Device Recalls
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1 result found
510(K) Number: K140205 |
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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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| Pleur-evac Chest Drainage System, Dry Suction/Dry Seal Control, REF A-6000-08LF, Rx Only, Teleflex M... | 2 | 04/28/2016 |
FEI # 3005747797 Teleflex Medical |
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