Clearance Summary
Phoenix XL Dialysate Meter received FDA 510(k) clearance under submission number K150657, sponsored by Mesa Laboratories, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Gastroenterology, Urology review panel. The statutory decision date of record is 2015-09-21.
- Submission: K150657
- Applicant / Sponsor: Mesa Laboratories, Inc.
- Clearance pathway: Traditional
- Review panel: Gastroenterology, Urology
- Device class: Class II
- Regulation citation: 21 CFR 876.5820
- Decision date: 2015-09-21
Classification & Regulation
This clearance is catalogued under FDA product code FIZ and 21 CFR 876.5820, within the Gastroenterology, Urology review panel as a Class II device.