Clearance Summary
MEDI-CULT SPERM PREPARATION - MEDIUM; received FDA 510(k) clearance under submission number K991332, sponsored by Medicult A/S. 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 2000-05-04.
- Submission: K991332
- Applicant / Sponsor: Medicult A/S
- Clearance pathway: Traditional
- Review panel: Obstetrics/Gynecology
- Device class: Class II
- Regulation citation: 21 CFR 884.6180
- Decision date: 2000-05-04
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.