Medical Device Recalls
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11 to 15 of 15 Results
510(K) Number: K050190 |
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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| Juno DRF , X-ray system, diagnostic, Fluoroscopic, general-purpose Model: 70920 Product Usage: ... | 2 | 01/28/2013 | Philips Healthcare Inc. |
| 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, Model Number 709020 - Product Usage: General. multi-function x-ray systems capable of rout... | 2 | 12/31/2019 | Villa Sistemi Medicali S.P.A. |
| 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 DRF; Model: 709020 Product Usage: General, multi-function x-ray systems capable of routine ... | 2 | 03/09/2017 | Villa Sistemi Medicali S.P.A. |
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