Clearance Summary
MEDOS HILITE 7000 & 7000 LT OXYGENATOR received FDA 510(k) clearance under submission number K133261, sponsored by Medos Medizintechnik AG. The device was reviewed via the Special premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2014-01-09.
- Submission: K133261
- Applicant / Sponsor: Medos Medizintechnik AG
- Clearance pathway: Special
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.4350
- Decision date: 2014-01-09
Classification & Regulation
This clearance is catalogued under FDA product code DTZ and 21 CFR 870.4350, within the Cardiovascular review panel as a Class II device.