Clearance Summary
MODIFICATION TO HERMES OPERATING ROOM CONTROL CENTER received FDA 510(k) clearance under submission number K003222, sponsored by Computer Motion, 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 2000-11-03.
- Submission: K003222
- Applicant / Sponsor: Computer Motion, Inc.
- Clearance pathway: Special
- Review panel: Gastroenterology, Urology
- Device class: Class II
- Regulation citation: 21 CFR 876.1500
- Decision date: 2000-11-03
Classification & Regulation
This clearance is catalogued under FDA product code GCI and 21 CFR 876.1500, within the Gastroenterology, Urology review panel as a Class II device.