Clearance Summary
Modulith SLX-F2 received FDA 510(k) clearance under submission number K201001, sponsored by Karl Storz Endoscopy America. 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 2021-03-30.
- Submission: K201001
- Applicant / Sponsor: Karl Storz Endoscopy America
- Clearance pathway: Traditional
- Review panel: Gastroenterology, Urology
- Device class: Class II
- Regulation citation: 21 CFR 876.5990
- Decision date: 2021-03-30
Classification & Regulation
This clearance is catalogued under FDA product code LNS and 21 CFR 876.5990, within the Gastroenterology, Urology review panel as a Class II device.