Clearance Summary
RIA LATEX CONDOM, NONOXYNOL-9 received FDA 510(k) clearance under submission number K945145, sponsored by Mbf Personal Care Sdn. Bhd.. 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 1996-02-21.
- Submission: K945145
- Applicant / Sponsor: Mbf Personal Care Sdn. Bhd.
- Clearance pathway: Traditional
- Review panel: Obstetrics/Gynecology
- Device class: Class II
- Regulation citation: 21 CFR 884.5300
- Decision date: 1996-02-21
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.