Clearance Summary
Panpac Flexi Shelf Pessary received FDA 510(k) clearance under submission number K173351, sponsored by Panpac Medical Corporation. The device was reviewed via the Abbreviated premarket notification pathway and assigned to the Obstetrics/Gynecology review panel. The statutory decision date of record is 2018-10-31.
- Submission: K173351
- Applicant / Sponsor: Panpac Medical Corporation
- Clearance pathway: Abbreviated
- Review panel: Obstetrics/Gynecology
- Device class: Class II
- Regulation citation: 21 CFR 884.3575
- Decision date: 2018-10-31
Classification & Regulation
This clearance is catalogued under FDA product code HHW and 21 CFR 884.3575, within the Obstetrics/Gynecology review panel as a Class II device.