Clearance Summary
PROTEX CONTRACEPT PLUS W/SPERM-LUB received FDA 510(k) clearance under submission number K831816, sponsored by National Sanitary Laboratories, Inc.. 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 1983-09-12.
- Submission: K831816
- Applicant / Sponsor: National Sanitary Laboratories, Inc.
- Clearance pathway: Traditional
- Review panel: Obstetrics/Gynecology
- Device class: Class II
- Regulation citation: 21 CFR 884.5300
- Decision date: 1983-09-12
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.