Clearance Summary
KARL STORZ DIRECT COUPLED CAMERA HEAD received FDA 510(k) clearance under submission number K973252, sponsored by Karl Storz Imaging, Inc.. 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 1997-11-24.
- Submission: K973252
- Applicant / Sponsor: Karl Storz Imaging, Inc.
- Clearance pathway: Traditional
- Review panel: Gastroenterology, Urology
- Device class: Class II
- Regulation citation: 21 CFR 876.1500
- Decision date: 1997-11-24
Classification & Regulation
This clearance is catalogued under FDA product code FET and 21 CFR 876.1500, within the Gastroenterology, Urology review panel as a Class II device.