Clearance Summary
ProNephro AKI (NGAL) received FDA 510(k) clearance under submission number K232761, sponsored by Bioporto Diagnostic, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Clinical Chemistry review panel. The statutory decision date of record is 2023-12-07.
- Submission: K232761
- Applicant / Sponsor: Bioporto Diagnostic, Inc.
- Clearance pathway: Traditional
- Review panel: Clinical Chemistry
- Device class: Class II
- Regulation citation: 21 CFR 862.1220
- Decision date: 2023-12-07
Classification & Regulation
This clearance is catalogued under FDA product code PIG and 21 CFR 862.1220, within the Clinical Chemistry review panel as a Class II device.