Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K212673 |
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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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MR 5300- Magnetic Resonance (MR) systems are Medical Electrical Systems indicated for use as a diag... | 2 | 05/17/2024 | Philips North America Llc |
MR 5300, Magnetic Resonance System. | 2 | 04/17/2024 | Philips North America Llc |
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