Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K201012 |
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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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Philips Ultrasound, Inc. Sparq, Diagnostic Ultrasound System, REF 795116, 100-240V -, 50/60 Hz, 500 ... | 2 | 10/07/2021 | Philips Ultrasound Inc |
Philips Ultrasound, Inc. Sparq, Diagnostic Ultrasound System, REF 795090, 100-240V -, 50/60 Hz, 500 ... | 2 | 10/07/2021 | Philips Ultrasound Inc |
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