Medical Device Recalls
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1 to 4 of 4 Results
510(K) Number: K060259 |
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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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Innova 2121-IQ/3131-IQ Biplane Cardiovascular Imaging System. The Innova Biplane systems are the fir... | 2 | 05/19/2009 | GE Medical Systems, LLC |
Innova 2121-IQ/3131-IQ Biplane Cardiovascular Imaging System. | 2 | 11/09/2009 | GE Medical Systems, LLC |
GE Healthcare, Innova 2121IQ, Innova 3131IQ Cardiovascular X-ray imaging systems. K060259: The Inno... | 2 | 09/13/2012 | GE Healthcare, LLC |
GE Healthcare, Innova 2121-1Q/3131-1Q Biplane Cardiovascular Imaging Systems. Indicated for use ... | 2 | 12/16/2009 | GE Medical Systems, LLC |
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