Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K952631 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Diapact CRRT Assembled Kit HF/HD with Manifold and Standard Spike, item number 7210513. The product ... | 3 | 05/07/2008 |
FEI # 2523676 B. Braun Medical, Inc. |
| Diapact CRRT Assembled Kit HF/HD with Manifold and Standard Spike, item number 7210517. The product ... | 3 | 05/07/2008 |
FEI # 2523676 B. Braun Medical, Inc. |
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