Medical Device Recalls
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1 result found
510(K) Number: K231764 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Ultrasound System 1300, bkSpecto w/battery; Model No. 1300-21 or 1300-S1; System, Imaging, Pulsed Do... | 2 | 11/06/2025 | B-K Medical A/S |
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