Clearance Summary
UNIDRIVE II PLUS DISPOSABLE TUBING SET received FDA 510(k) clearance under submission number K021811, sponsored by Mtp Medical Technical Promotion GmbH. The device was reviewed via the Traditional premarket notification pathway and assigned to the Ear, Nose, Throat review panel. The statutory decision date of record is 2002-06-19.
- Submission: K021811
- Applicant / Sponsor: Mtp Medical Technical Promotion GmbH
- Clearance pathway: Traditional
- Review panel: Ear, Nose, Throat
- Device class: Class II
- Regulation citation: 21 CFR 874.4250
- Decision date: 2002-06-19
Classification & Regulation
This clearance is catalogued under FDA product code ERL and 21 CFR 874.4250, within the Ear, Nose, Throat review panel as a Class II device.