Zevex Incorporated (dba MOOG Medical Devices Group)
2 FDA 510(k) clearances · Recalling firm
◉ Watch Zevex Incorporated (dba MOOG Medical Devices Group)
| Record | Firm | Date |
|---|---|---|
| MOOG Curlin Infusion Administration Set, REF 340-4130, Non-DEHP Tubing with Non-Vented Bag recall (Z-2053-2019) | Zevex Incorporated (dba MOOG Medical Devices Group) | 2019-07-23 |
| MOOG Curlin Infusion Administration Set, REF 340-4130-V, Non-DEHP Tubing with Non-Vented B recall (Z-2054-2019) | Zevex Incorporated (dba MOOG Medical Devices Group) | 2019-07-23 |
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Every clearance here is in the API, with alerts when new ones post.