Clearance Summary
MODULEAF received FDA 510(k) clearance under submission number K030609, sponsored by Mrc Systems 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 2003-03-17.
- Submission: K030609
- Applicant / Sponsor: Mrc Systems GmbH
- Clearance pathway: Special
- Review panel: Radiology
- Device class: Class II
- Regulation citation: 21 CFR 892.5710
- Decision date: 2003-03-17
Classification & Regulation
This clearance is catalogued under FDA product code IXI and 21 CFR 892.5710, within the Radiology review panel as a Class II device.