Medical Device Recalls
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11 to 12 of 12 Results
510(K) Number: K010817 |
Results per Page |
Product Description
|
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 |
Philips MX8000 Dual v. EXP CT Scanner, utilizing V2.0 software. | 3 | 05/15/2003 | Philips Medical Systems (Cleveland) Inc |
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