Clearance Summary
KION ANAESTHESIA SYSTEM, MODEL 65 03 879 E392E received FDA 510(k) clearance under submission number K010923, sponsored by Siemens Elema AB. The device was reviewed via the Abbreviated premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2002-01-23.
- Submission: K010923
- Applicant / Sponsor: Siemens Elema AB
- Clearance pathway: Abbreviated
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.1025
- Decision date: 2002-01-23
Classification & Regulation
This clearance is catalogued under FDA product code MHX and 21 CFR 870.1025, within the Cardiovascular review panel as a Class II device.