Clearance Summary
ROSTAM APPLICATOR TAMPON/ROSTAM NON APPLICATOR TAMPON received FDA 510(k) clearance under submission number K965064, sponsored by Rostam , Ltd.. 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 1997-02-20.
- Submission: K965064
- Applicant / Sponsor: Rostam , Ltd.
- Clearance pathway: Traditional
- Review panel: Obstetrics/Gynecology
- Device class: Class II
- Regulation citation: 21 CFR 884.5470
- Decision date: 1997-02-20
Classification & Regulation
This clearance is catalogued under FDA product code HEB and 21 CFR 884.5470, within the Obstetrics/Gynecology review panel as a Class II device.