Clearance Summary
FLEXIVIEW 8800 DIGITAL MOBILE IMAGING SYSTEM received FDA 510(k) clearance under submission number K003837, sponsored by Ge Oec Medical Systems. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2001-03-12.
- Submission: K003837
- Applicant / Sponsor: Ge Oec Medical Systems
- Clearance pathway: Traditional
- Review panel: Radiology
- Device class: Class II
- Regulation citation: 21 CFR 892.1650
- Decision date: 2001-03-12
Classification & Regulation
This clearance is catalogued under FDA product code OXO and 21 CFR 892.1650, within the Radiology review panel as a Class II device.