Medical Device Recalls
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31 to 34 of 34 Results
510(K) Number: K042053 |
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
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GE Healthcare Innova 4100/4100 IQ. Digital Fluoroscopic Imaging System (Vascular Angiography System... | 2 | 06/05/2007 | General Electric Med Systems LLC |
GE Healthcare Innova 3100/ 3100 IQ Digital Fluoroscopic Imaging System (Cardiovascular Imaging Syst... | 2 | 07/10/2007 | General Electric Med Systems LLC |
GE Healthcare Innova 3100/ 3100 IQ Digital Fluoroscopic Imaging System (Cardiovascular Imaging Sys... | 2 | 06/05/2007 | General Electric Med Systems LLC |
GE Healthcare Innova 2100 IQ Digital Fluoroscopic Imaging System (Versatile cardiac and vascular) | 2 | 06/05/2007 | General Electric Med Systems LLC |
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