Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K061203 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Ziehm Vision R. Iterventional fluoroscopic x-ray system | 2 | 12/02/2024 |
FEI # 3005254598 Orthoscan, Inc. |
| Ziehm Vision R, Mobile C-arm for Mobile Fluoroscopic Imaging | 2 | 08/25/2016 |
FEI # 2027299 Ziehm Imaging Inc |
| Ziehm Vision R C-Arm Interventional Fluoroscopic X-Ray System. Mobile Fluoroscopic Imaging | 2 | 12/24/2013 |
FEI # 2027299 Ziehm Imaging Inc |
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