Medical Device Recalls
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1 result found
510(K) Number: K873296 |
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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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| GE Healthcare Lunar: a) DPX NT, Model Numbers: LU8230, LU40338, LU42357, LU42369 b) DPX MD+, Mode... | 2 | 04/17/2018 |
FEI # 2183066 GE Medical Systems Ultrasound & Primary Care Diagnostics, LL |
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