Medical Device Recalls
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31 to 31 of 31 Results
510(K) Number: K952516 |
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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| Portex Custom Pro-Vent Arterial Blood Sampling Kit Catalog Number: G1540 | 2 | 11/24/2004 |
FEI # 1217052 Smiths Medical ASD, Inc. |
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