Medical Device Recalls
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1 to 5 of 5 Results
510(K) Number: K041931 |
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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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| GE OEC 9900 Elite Digital Mobile C-Arm X-ray system, GE OEC Medical Systems Inc. | 2 | 09/30/2006 | GE OEC Medical Systems, Inc |
| GE OEC 9900 Elite Fluoroscopic X-ray System, GE Healthcare, Salt Lake City, Utah. | 2 | 06/30/2007 | GE OEC Medical Systems, Inc |
| GE OEC 9900 Elite Fluoroscopy System with Integrated Navigation,GE OEC Medical Systems Inc. | 2 | 10/25/2006 | GE OEC Medical Systems, Inc |
| GEHC OEC 9900 ESP-15 Elite C-Arm fluoroscopic X-ray system, GE Healthcare, Salt Lake City, UT. | 2 | 07/12/2007 | GE OEC Medical Systems, Inc |
| OEC 9900 Elite Fluoroscopy System, Catalog No. 887208 and 887210, GE OEC Medical Systems, Inc. | 2 | 10/14/2006 | GE OEC Medical Systems, Inc |
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