Clearance Summary
FLEXILOG 3000 received FDA 510(k) clearance under submission number K964589, sponsored by Oakfield Instruments, Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Gastroenterology, Urology review panel. The statutory decision date of record is 1997-03-04.
- Submission: K964589
- Applicant / Sponsor: Oakfield Instruments, Ltd.
- Clearance pathway: Traditional
- Review panel: Gastroenterology, Urology
- Device class: Class II
- Regulation citation: 21 CFR 876.1725
- Decision date: 1997-03-04
Classification & Regulation
This clearance is catalogued under FDA product code KLA and 21 CFR 876.1725, within the Gastroenterology, Urology review panel as a Class II device.