Medical Device Recalls
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21 to 22 of 22 Results
510(K) Number: K050228 |
Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Agfa HeartLab Cardiovascular DICOMstore Version 2.04.40.00 software, Heartlab, Inc., Wester... | 2 | 06/27/2008 | AGFA Corp. |
Agfa IMPAX CardioVascular Suite Results Management Nuclear Reporting Module, Outbound Report, Model/... | 2 | 03/31/2008 | AGFA Corp. |
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