Clearance Summary
PADS MENSTRUAL, UNTREAT DEODORIZED, VARIOUS SIZES received FDA 510(k) clearance under submission number K933879, sponsored by Universal Health Care Products Canada, 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 1994-03-24.
- Submission: K933879
- Applicant / Sponsor: Universal Health Care Products Canada, Inc.
- Clearance pathway: Traditional
- Review panel: Obstetrics/Gynecology
- Device class: Class I
- Regulation citation: 21 CFR 884.5435
- Decision date: 1994-03-24
Classification & Regulation
This clearance is catalogued under FDA product code HHD and 21 CFR 884.5435, within the Obstetrics/Gynecology review panel as a Class I device.