Clearance Summary
ONCE TM received FDA 510(k) clearance under submission number K800162, sponsored by G.D. Searle and Co.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Obstetrics/Gynecology review panel. The statutory decision date of record is 1980-02-11.
- Submission: K800162
- Applicant / Sponsor: G.D. Searle and Co.
- Clearance pathway: Traditional
- Review panel: Obstetrics/Gynecology
- Device class: Class II
- Regulation citation: 21 CFR 884.5350
- Decision date: 1980-02-11
Classification & Regulation
This clearance is catalogued under FDA product code HDW and 21 CFR 884.5350, within the Obstetrics/Gynecology review panel as a Class II device.