Clearance Summary
Medline ReNewal Reprocessed OxiMax Pulse Oximetry Sensors received FDA 510(k) clearance under submission number K181738, sponsored by Surgical Instrument Service and Savings Inc (Dba Medline. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2019-03-22.
- Submission: K181738
- Applicant / Sponsor: Surgical Instrument Service and Savings Inc (Dba Medline
- Clearance pathway: Traditional
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.2700
- Decision date: 2019-03-22
Classification & Regulation
This clearance is catalogued under FDA product code DQA and 21 CFR 870.2700, within the Cardiovascular review panel as a Class II device.