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U.S. Department of Health and Human Services

Medical Device Recalls
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510(K) Number: K140783
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Nimbus II Infusion System; Nimbus II PainPRO IT1053; Nimbus II Flex IT1062; Nimbus II Plus IT107... 1 03/28/2024 InfuTronix LLC
Nimbus Administration Set; Nimbus Flex; Nimbus PainPro (a.k.a. Halo Ambulatory Infusion System); ... 1 03/28/2024 InfuTronix LLC
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