Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K092004 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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GE Healthcare, Innova 2100 IQ, Innova 3100 IQ, Innova 4100 IQ. Cardiovascular X-ray imaging systems... | 2 | 03/11/2013 | GE Healthcare, LLC |
GE Healthcare, Innova® 3100IQ (Optima Edition) Fluoroscopic Vascular X-ray System. Indicated for ... | 2 | 10/28/2011 | GE Healthcare, LLC |
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