Clearance Summary
PICASSO MASTER, ECT AND MASTER 3D received FDA 510(k) clearance under submission number K081847, sponsored by E-Woo Technology. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2008-08-21.
- Submission: K081847
- Applicant / Sponsor: E-Woo Technology
- Clearance pathway: Traditional
- Review panel: Radiology
- Device class: Class II
- Regulation citation: 21 CFR 892.1750
- Decision date: 2008-08-21
Classification & Regulation
This clearance is catalogued under FDA product code JAK and 21 CFR 892.1750, within the Radiology review panel as a Class II device.