Clearance Summary
BESTCON/SPERMICIDE received FDA 510(k) clearance under submission number K871451, sponsored by Europharmaceutical Corp.. 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 1987-12-08.
- Submission: K871451
- Applicant / Sponsor: Europharmaceutical Corp.
- Clearance pathway: Traditional
- Review panel: Obstetrics/Gynecology
- Device class: Class II
- Regulation citation: 21 CFR 884.5300
- Decision date: 1987-12-08
Classification & Regulation
This clearance is catalogued under FDA product code HIS and 21 CFR 884.5300, within the Obstetrics/Gynecology review panel as a Class II device.