Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K050751 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| IMPAX® 4.1, IMPAX ® 4.5, IMPAX ® 5.0, IMPAX ® 5.1 IMPAX ® 5.2, IMPAX ® 6.0, IMPAX ® 6.2; Picture Arc... | 2 | 09/11/2008 | AGFA Corp. |
| WEB1000 Versions 3.1, 4.1 and 5.1, Picture Archiving and Communications systems (PACs), used in the ... | 2 | 09/11/2008 | AGFA Corp. |
| IMPAX® 6.2.1 System, Picture Archiving and Communications system (PAC), used in the acceptance, tran... | 2 | 09/11/2008 | AGFA Corp. |
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