Clearance Summary
Möller Medical Biopsy Needles and Systems received FDA 510(k) clearance under submission number K162588, sponsored by Moller Medical GmbH. 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 2017-06-19.
- Submission: K162588
- Applicant / Sponsor: Moller Medical GmbH
- Clearance pathway: Traditional
- Review panel: Gastroenterology, Urology
- Device class: Class II
- Regulation citation: 21 CFR 876.1075
- Decision date: 2017-06-19
Classification & Regulation
This clearance is catalogued under FDA product code KNW and 21 CFR 876.1075, within the Gastroenterology, Urology review panel as a Class II device.