Clearance Summary
Novalung ultimate kit (US) received FDA 510(k) clearance under submission number K232926, sponsored by Fresenius Medical Care Renal Therapies Group, LLC. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2024-04-15.
- Submission: K232926
- Applicant / Sponsor: Fresenius Medical Care Renal Therapies Group, LLC
- Clearance pathway: Traditional
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.4100
- Decision date: 2024-04-15
Classification & Regulation
This clearance is catalogued under FDA product code QJZ and 21 CFR 870.4100, within the Cardiovascular review panel as a Class II device.