Clearance Summary
PVP, POLYVINYLPYRROLIDONE 10% (W/V) IN HEPES-HTF received FDA 510(k) clearance under submission number K991391, sponsored by Advanced Reproductive Technologies. 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 2000-01-10.
- Submission: K991391
- Applicant / Sponsor: Advanced Reproductive Technologies
- Clearance pathway: Traditional
- Review panel: Obstetrics/Gynecology
- Device class: Class II
- Regulation citation: 21 CFR 884.6180
- Decision date: 2000-01-10
Classification & Regulation
This clearance is catalogued under FDA product code MQL and 21 CFR 884.6180, within the Obstetrics/Gynecology review panel as a Class II device.