Clearance Summary
PULSEOX 5500 FINGER DEVICE, PULSEOX 7500 WRISTWATCH DEVICE received FDA 510(k) clearance under submission number K040178, sponsored by S.P.O. Medical Equipment, Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2004-09-10.
- Submission: K040178
- Applicant / Sponsor: S.P.O. Medical Equipment, Ltd.
- Clearance pathway: Traditional
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.2700
- Decision date: 2004-09-10
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.