Medical Device Recalls
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1 to 4 of 4 Results
510(K) Number: K101517 |
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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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| Digital Mobile X-ray Systems used to take diagnostic radiographic exposures or patients. | 2 | 02/09/2015 |
FEI # 3011066290 Virtual Imaging, Inc. |
| RadPRO(R) Mobile 40kW Digital X-Ray System - Model: SM-40HF-B-D-C Product Usage: Instrument i... | 2 | 11/14/2018 |
FEI # 1000649926 Virtual Imaging, Inc. |
| RadPro 40kW Digital X-Ray Panel and Mobile/Portable Diagnostic X-Ray. Intended for use by a quali... | 2 | 08/14/2015 |
FEI # 3002495042 Sedecal S.A. |
| Sedecal Mobile Digital Diagnostic X-Ray Systems; SM-40HF-B-D-KM (AeroDR X30) | 2 | 10/23/2025 |
FEI # 3002495042 SEDECAL SA |
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