Clearance Summary
PRISMAFLO received FDA 510(k) clearance under submission number K020103, sponsored by Stihler Electronic GmbH. The device was reviewed via the Abbreviated premarket notification pathway and assigned to the Gastroenterology, Urology review panel. The statutory decision date of record is 2002-07-24.
- Submission: K020103
- Applicant / Sponsor: Stihler Electronic GmbH
- Clearance pathway: Abbreviated
- Review panel: Gastroenterology, Urology
- Device class: Class II
- Regulation citation: 21 CFR 876.5820
- Decision date: 2002-07-24
Classification & Regulation
This clearance is catalogued under FDA product code KOC and 21 CFR 876.5820, within the Gastroenterology, Urology review panel as a Class II device.