Medical Device Recalls
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1 result found
510(K) Number: K220800 |
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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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Venue Go Standard Carts Ref: (H45181VC and H45103VCW), used with Venue Go R2, R3, R4 systems R2, R3,... | 2 | 09/29/2023 | GE MEDICAL SYSTEMS, ISRAEL LTD. |
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