Clearance Summary
Go Dose System received FDA 510(k) clearance under submission number K160949, sponsored by Eli Lilly and Company. The device was reviewed via the Traditional premarket notification pathway and assigned to the Anesthesiology review panel. The statutory decision date of record is 2016-12-22.
- Submission: K160949
- Applicant / Sponsor: Eli Lilly and Company
- Clearance pathway: Traditional
- Review panel: Anesthesiology
- Device class: Class II
- Regulation citation: 21 CFR 868.1890
- Decision date: 2016-12-22
Classification & Regulation
This clearance is catalogued under FDA product code NDC and 21 CFR 868.1890, within the Anesthesiology review panel as a Class II device.