Medical Device Recalls
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11 to 14 of 14 Results
510(K) Number: K052412 |
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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| GE Innova 2100IQ Versatile Cardiac and Vascular Imaging System, GE Healthcare, Waukesha, WI 53188 ( ... | 2 | 09/21/2008 |
FEI # 2126677 GE Healthcare |
| GE Innova 3100 / 3100 IQ, Cardiovascular Imaging System, GE Healthcare, Waukesha, WI 53188 (The syst... | 2 | 09/21/2008 |
FEI # 2126677 GE Healthcare |
| GE Innova 4100 / 4100 IQ. , GE Healthcare, Waukesha, WI 53188 ( The system consists of an a monoplan... | 2 | 09/21/2008 |
FEI # 2126677 GE Healthcare |
| GE Healthcare Innova 2100 IQ Digital Fluoroscopic Imaging System (Versatile cardiac and vascular ima... | 2 | 06/09/2007 |
FEI # 2126677 General Electric Med Systems LLC |
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