Clearance Summary
KSEA VAPORIZATION ELECTRODES received FDA 510(k) clearance under submission number K961702, sponsored by Karl Storz Endoskop GmbH. 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 1996-08-29.
- Submission: K961702
- Applicant / Sponsor: Karl Storz Endoskop GmbH
- Clearance pathway: Traditional
- Review panel: Gastroenterology, Urology
- Device class: Class II
- Regulation citation: 21 CFR 876.4300
- Decision date: 1996-08-29
Classification & Regulation
This clearance is catalogued under FDA product code FAS and 21 CFR 876.4300, within the Gastroenterology, Urology review panel as a Class II device.