Medical Device Recalls
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1 result found
510(K) Number: K103551 |
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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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A) Product Code 2N8220: Non-DEHP Catheter Extension Set Kit, Single use only, includes: 1) 7.7", Vo... | 2 | 05/07/2013 | Baxter Healthcare Corp. |
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