Medical Device Recalls
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11 to 12 of 12 Results
510(K) Number: K010817 |
Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Brillance CT System, 16 Power configuration using version 1.2 or 1.2.1 software. | 2 | 08/30/2005 | Philips Medical Systems (Cleveland) Inc |
Brillance CT System, 16, 10 and 6 configurations (air cooled version) using version 1.2 or 1.2.1soft... | 2 | 08/30/2005 | Philips Medical Systems (Cleveland) Inc |
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