Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K790006 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Ultrasite IV Administration Set with Universal Spike, three Backcheck Valves, three Ultrasite Inject... | 2 | 06/05/2009 |
FEI # 2523676 B. Braun Medical, Inc. |
| IV Administration Set with Universal Spike, two Ultrasite Injection Sites, Backcheck Valve and Spin-... | 2 | 06/05/2009 |
FEI # 2523676 B. Braun Medical, Inc. |
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