Clearance Summary
PHOENIX DIALYSATE METER received FDA 510(k) clearance under submission number K955298, sponsored by Automata Medical Instrumentation, 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 1996-02-29.
- Submission: K955298
- Applicant / Sponsor: Automata Medical Instrumentation, Inc.
- Clearance pathway: Traditional
- Review panel: Gastroenterology, Urology
- Device class: Class II
- Regulation citation: 21 CFR 876.5820
- Decision date: 1996-02-29
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.