Clearance Summary
MODULTH SLK received FDA 510(k) clearance under submission number K120769, sponsored by KARL STORZ Endoscopy-America, Inc.. 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 2012-06-12.
- Submission: K120769
- Applicant / Sponsor: KARL STORZ Endoscopy-America, Inc.
- Clearance pathway: Special
- Review panel: Gastroenterology, Urology
- Device class: Class II
- Regulation citation: 21 CFR 876.5990
- Decision date: 2012-06-12
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.