InfuTronix LLC
3 FDA 510(k) clearances · Recalling firm
| Record | Firm | Date |
|---|---|---|
| Nimbus Administration Set; Nimbus Flex; Nimbus PainPro (a.k.a. Halo Ambulatory Infusion Sy recall (Z-1285-2024) | InfuTronix LLC | 2024-03-28 |
| Nimbus II Infusion System; Nimbus II PainPRO IT1053; Nimbus II Flex IT1062; Nimbus II Plus recall (Z-1286-2024) | InfuTronix LLC | 2024-03-28 |
| Nimbus Administration Set, REF HS-004, UDI # 00817170020031 Product Usage: Administer flui recall (Z-2055-2019) | InfuTronix LLC | 2019-07-23 |
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Every clearance here is in the API, with alerts when new ones post.