Clearance Summary
CABOT MEDICAL NIAGARA(TM) 3.0 LITER HIGH FLOW IRRI received FDA 510(k) clearance under submission number K924530, sponsored by Cabot Medical Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Obstetrics/Gynecology review panel. The statutory decision date of record is 1993-02-05.
- Submission: K924530
- Applicant / Sponsor: Cabot Medical Corp.
- Clearance pathway: Traditional
- Review panel: Obstetrics/Gynecology
- Device class: Class II
- Regulation citation: 21 CFR 884.1720
- Decision date: 1993-02-05
Classification & Regulation
This clearance is catalogued under FDA product code HET and 21 CFR 884.1720, within the Obstetrics/Gynecology review panel as a Class II device.