Medical Device Recalls
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11 to 11 of 11 Results
510(K) Number: K061289 |
Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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4FR Single Lumen Pressure Injectable PICC; intravascular therapeutic catheter, for long-term use gr... | 2 | 10/15/2015 | Arrow International Inc |
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