Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K061284 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Gendex CB-500, 3D Dental Imaging Systems, Model Number G1-15-1-0. This product is manufactured by I... | 2 | 05/22/2009 |
FEI # 3021551875 Imaging Sciences International, LLC |
| i-CAT 17-19 Cone Beam 3D Dental Imaging System. This product is also sold under a private label as K... | 2 | 09/01/2008 |
FEI # 3021551875 Imaging Sciences Intl Inc |
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