Clearance Summary
MULTI PURPOSE FLEX ARRAY COIL : MODEL 235 SERIES received FDA 510(k) clearance under submission number K000345, sponsored by Medical Advances, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2000-04-11.
- Submission: K000345
- Applicant / Sponsor: Medical Advances, Inc.
- Clearance pathway: Traditional
- Review panel: Radiology
- Device class: Class II
- Regulation citation: 21 CFR 892.1000
- Decision date: 2000-04-11
Classification & Regulation
This clearance is catalogued under FDA product code MOS and 21 CFR 892.1000, within the Radiology review panel as a Class II device.