Medical Device Recalls
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1 to 4 of 4 Results
510(K) Number: K112670 |
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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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DX-D 600 DIRECT RADIOGRAPHY SYSTEM Product Usage: The DX-D 600 system is a ceiling mounted Gener... | 2 | 01/07/2019 | Agfa-Gevaert, N.V. |
DX-D 600 Product Usage: The DX-D 600 system is a ceiling mounted General Radiography X-Ray imagi... | 2 | 09/25/2018 | Agfa N.V. |
DX-D600 - DXD Imaging Package | 2 | 04/05/2017 | AGFA Healthcare Corp. |
DX-D 600 - DXD Imaging Package Product Usage:Is indicated for use in providing diagnostic quality... | 2 | 08/10/2014 | AGFA Healthcare Corp. |
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