Clearance Summary
REPROCESSED MASIMO PULSE OXIMETER SENSORS received FDA 510(k) clearance under submission number K081238, sponsored by Ascent Healthcare Solutions. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2008-07-29.
- Submission: K081238
- Applicant / Sponsor: Ascent Healthcare Solutions
- Clearance pathway: Traditional
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.2700
- Decision date: 2008-07-29
Classification & Regulation
This clearance is catalogued under FDA product code NLF and 21 CFR 870.2700, within the Cardiovascular review panel as a Class II device.