Clearance Summary
FLEXILOG 2000 received FDA 510(k) clearance under submission number K945069, 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 1995-06-13.
- Submission: K945069
- Applicant / Sponsor: Oakfield Instruments, Ltd.
- Clearance pathway: Traditional
- Review panel: Gastroenterology, Urology
- Device class: Class I
- Regulation citation: 21 CFR 876.1400
- Decision date: 1995-06-13
Classification & Regulation
This clearance is catalogued under FDA product code FFT and 21 CFR 876.1400, within the Gastroenterology, Urology review panel as a Class I device.