Clearance Summary
DATEX-OHMEDA S/5 WEB VIEWER WITH L-6WV02 SOFTWARE received FDA 510(k) clearance under submission number K023497, sponsored by Datex-Ohmeda. The device was reviewed via the Special premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2002-11-04.
- Submission: K023497
- Applicant / Sponsor: Datex-Ohmeda
- Clearance pathway: Special
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.2300
- Decision date: 2002-11-04
Classification & Regulation
This clearance is catalogued under FDA product code MSX and 21 CFR 870.2300, within the Cardiovascular review panel as a Class II device.