Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K093318 |
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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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Accelerator APS Aliquoter Module, List number: 07L40 - Product Usage: The ACCELERATOR APS Workcell i... | 2 | 06/03/2020 | Abbott Laboratories |
APS Accelerator modular systems, 208-230 V-, 50/60 Hz, 1800 VA, IVD, RX, Class 2 Laser Product, | 2 | 09/26/2019 | Abbott Laboratories, Inc |
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