Clearance Summary
ULTRACONCENTRATOR SYSTEM received FDA 510(k) clearance under submission number K011148, sponsored by Interpore Cross Intl.. The device was reviewed via the Special premarket notification pathway and assigned to the Gastroenterology, Urology review panel. The statutory decision date of record is 2001-06-13.
- Submission: K011148
- Applicant / Sponsor: Interpore Cross Intl.
- Clearance pathway: Special
- Review panel: Gastroenterology, Urology
- Device class: Class II
- Regulation citation: 21 CFR 876.5820
- Decision date: 2001-06-13
Classification & Regulation
This clearance is catalogued under FDA product code FJI and 21 CFR 876.5820, within the Gastroenterology, Urology review panel as a Class II device.