Clearance Summary
PS SERIES received FDA 510(k) clearance under submission number K061622, sponsored by Photonic Optische Gerate Gesmbh & Cokg. 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 2007-03-05.
- Submission: K061622
- Applicant / Sponsor: Photonic Optische Gerate Gesmbh & Cokg
- Clearance pathway: Traditional
- Review panel: Gastroenterology, Urology
- Device class: Class II
- Regulation citation: 21 CFR 876.1500
- Decision date: 2007-03-05
Classification & Regulation
This clearance is catalogued under FDA product code FFS and 21 CFR 876.1500, within the Gastroenterology, Urology review panel as a Class II device.