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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Philips MX8000 Dual v. EXP CT Scanner, utilizing V2.0 software. | 3 | 05/15/2003 | Philips Medical Systems (Cleveland) Inc |
Continuous CT Fluoroscopy DVI Ceiling Mount CCT Arm DVI Option - Monitor Bracket Assembly for use ... | 2 | 06/30/2021 | Philips North America Llc |
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