Clearance Summary
MOLINEA INCONTINENT PAD received FDA 510(k) clearance under submission number K843404, sponsored by Paul Hartmann Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Gastroenterology, Urology review panel. The statutory decision date of record is 1984-10-19.
- Submission: K843404
- Applicant / Sponsor: Paul Hartmann Corp.
- Clearance pathway: Traditional
- Review panel: Gastroenterology, Urology
- Device class: Class I
- Regulation citation: 21 CFR 876.5920
- Decision date: 1984-10-19
Classification & Regulation
This clearance is catalogued under FDA product code EYQ and 21 CFR 876.5920, within the Gastroenterology, Urology review panel as a Class I device.