Clearance Summary
LEO 7000 QUADRATURE KNEE COIL received FDA 510(k) clearance under submission number K971246, sponsored by Usa Instruments, 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 1997-06-20.
- Submission: K971246
- Applicant / Sponsor: Usa Instruments, Inc.
- Clearance pathway: Traditional
- Review panel: Radiology
- Device class: Class II
- Regulation citation: 21 CFR 892.1000
- Decision date: 1997-06-20
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.