Medical Device Recalls
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11 to 15 of 15 Results
510(K) Number: K050190 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Apollo: Models: 9784000131, 9784000231, 9784020131, 9784020231, 9784100231, 9784120131, 9784120231, ... | 2 | 01/20/2017 | Villa Radiology Systems LLC |
| Juno DRF; Model: 709020 Multi-function x-ray systems capable of routine radiograph and general fl... | 2 | 01/20/2017 | Villa Radiology Systems LLC |
| Juno DFR X-ray system | 2 | 03/06/2015 | Villa Radiology Systems LLC |
| Juno DRF System. Mobile X-ray system These are general, multi-function x-ray systems capable of r... | 2 | 09/13/2013 | Villa Radiology Systems LLC |
| Juno DRF , X-ray system, diagnostic, Fluoroscopic, general-purpose Model: 70920 Product Usage: ... | 2 | 01/28/2013 | Philips Healthcare Inc. |
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