Clearance Summary
Aquilex Fluid Control System AQL-100S received FDA 510(k) clearance under submission number K172040, sponsored by W.O.M. World of Medicine GmbH. The device was reviewed via the Special premarket notification pathway and assigned to the Obstetrics/Gynecology review panel. The statutory decision date of record is 2018-02-05.
- Submission: K172040
- Applicant / Sponsor: W.O.M. World of Medicine GmbH
- Clearance pathway: Special
- Review panel: Obstetrics/Gynecology
- Device class: Class II
- Regulation citation: 21 CFR 884.1700
- Decision date: 2018-02-05
Classification & Regulation
This clearance is catalogued under FDA product code HIG and 21 CFR 884.1700, within the Obstetrics/Gynecology review panel as a Class II device.