Medical Device Recalls
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1 to 4 of 4 Results
510(K) Number: K070528 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Philips Essenta DR, X-Ray System, Diagnostic, general-purpose Model: 712070. The Essenta DR is a... | 2 | 08/15/2012 |
FEI # 1218950 Philips Healthcare Inc. |
| Essenta DR is a digital multifunctional X-ray systems, suitable for all routine radiographic exams, ... | 2 | 10/06/2010 |
FEI # 1000524572 Philips Medical Systems North America Co. Phillips |
| Essenta DR - digital multifunctional x-ray system (application SW release 1.0.2 and lower). The dev... | 3 | 09/16/2008 |
FEI # 1000524572 Philips Medical Systems North America Co. Phillips |
| Philips Essenta DR, a Stationary x-ray system, X-ray system Model: 712070 The Essenta DR is a m... | 2 | 12/27/2013 |
FEI # 1218950 Philips Medical Systems, Inc. |
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