Medical Device Recalls
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11 to 12 of 12 Results
510(K) Number: K965240 |
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
Synchron CX Systems version 4.0 Operating Software used in Synchron LX20 Systems, Synchron LX20 Pro ... | 2 | 11/06/2003 | Beckman Coulter Inc |
SYNCHRON LX20 AND LX20 Pro | 2 | 02/05/2003 | Beckman Coulter Inc |
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