Clearance Summary
LIF-O-GEN #3000 OXYGEN CONCENTRATOR received FDA 510(k) clearance under submission number K812693, sponsored by Lif-O-Gen, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Anesthesiology review panel. The statutory decision date of record is 1981-10-13.
- Submission: K812693
- Applicant / Sponsor: Lif-O-Gen, Inc.
- Clearance pathway: Traditional
- Review panel: Anesthesiology
- Device class: Class II
- Regulation citation: 21 CFR 868.5440
- Decision date: 1981-10-13
Classification & Regulation
This clearance is catalogued under FDA product code CAW and 21 CFR 868.5440, within the Anesthesiology review panel as a Class II device.