Medical Device Recalls
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21 to 21 of 21 Results
510(K) Number: K993691 |
Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Arrowg+ard Blue Two Lumen CVC Super Kit, Catalog number AK-22802-SK. The kit actually contains Arrow... | 3 | 10/28/2004 | Arrow International Inc |
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