Medical Device Recalls
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1 to 5 of 5 Results
510(K) Number: K945945 |
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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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T5-NT, Model 78104 Product Usage: Indicated for use as a diagnostic device. It can produce cross... | 2 | 04/18/2018 | Philips Electronics North America Corporation |
ACS-NT, Model 78108 Product Usage: Indicated for use as a diagnostic device. It can produce cros... | 2 | 04/18/2018 | Philips Electronics North America Corporation |
T10-NT, Model 78107 Product Usage: Indicated for use as a diagnostic device. It can produce cros... | 2 | 04/18/2018 | Philips Electronics North America Corporation |
SENSE Body Coil 1.5T with identification; used in the ACS NT, Intera 1.5T and Achieva 1.5T MR syste... | 2 | 02/26/2016 | Philips Electronics North America Corporation |
Gyroscan MRI | 2 | 06/27/2007 | Philips Medical Systems North America Co. Phillips |
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