Clearance Summary
INTRABEAM SYSTEM received FDA 510(k) clearance under submission number K051055, sponsored by Carl Zeiss Surgical GmbH. The device was reviewed via the Special premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2005-05-23.
- Submission: K051055
- Applicant / Sponsor: Carl Zeiss Surgical GmbH
- Clearance pathway: Special
- Review panel: Radiology
- Device class: Class II
- Regulation citation: 21 CFR 892.5900
- Decision date: 2005-05-23
Classification & Regulation
This clearance is catalogued under FDA product code JAD and 21 CFR 892.5900, within the Radiology review panel as a Class II device.