Medical Device Recalls
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1 result found
510(K) Number: K221081 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| First Source iQ Flex M. Portable cart and platform that supports an X-ray system and laptop computer... | 2 | 07/01/2024 |
FEI # 3004063527 First Source Inc |
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