Clearance Summary
MOBILETTE XP AND MOBILETT XPHYBRID received FDA 510(k) clearance under submission number K033238, sponsored by Siemens Medical Systems, Inc.. The device was reviewed via the Special premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2003-11-14.
- Submission: K033238
- Applicant / Sponsor: Siemens Medical Systems, Inc.
- Clearance pathway: Special
- Review panel: Radiology
- Device class: Class II
- Regulation citation: 21 CFR 892.1720
- Decision date: 2003-11-14
Classification & Regulation
This clearance is catalogued under FDA product code IZL and 21 CFR 892.1720, within the Radiology review panel as a Class II device.