Clearance Summary
PERIFORM PERINEOMETRIC PROBE, MODEL 8300 received FDA 510(k) clearance under submission number K002617, sponsored by Neen Design , 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 2001-04-05.
- Submission: K002617
- Applicant / Sponsor: Neen Design , Ltd.
- Clearance pathway: Traditional
- Review panel: Obstetrics/Gynecology
- Device class: Class II
- Regulation citation: 21 CFR 884.1425
- Decision date: 2001-04-05
Classification & Regulation
This clearance is catalogued under FDA product code HIR and 21 CFR 884.1425, within the Obstetrics/Gynecology review panel as a Class II device.