Clearance Summary
CHLAMYDIA KIT, STD KIT received FDA 510(k) clearance under submission number K862322, sponsored by Intl. Cytobrush, 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 1986-07-07.
- Submission: K862322
- Applicant / Sponsor: Intl. Cytobrush, Inc.
- Clearance pathway: Traditional
- Review panel: Obstetrics/Gynecology
- Device class: Class II
- Regulation citation: 21 CFR 884.4530
- Decision date: 1986-07-07
Classification & Regulation
This clearance is catalogued under FDA product code HHT and 21 CFR 884.4530, within the Obstetrics/Gynecology review panel as a Class II device.