Medical Device Recalls
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1 result found
510(K) Number: K882329 |
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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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| Coiled 60" Low Pressure Extension Tube 400 PSI Max; packaged in Plastic and Tyvec pouch, with 100 po... | 2 | 02/29/2012 |
FEI # 1518293 Mallinckrodt Inc |
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