Clearance Summary
RMX PHYSIOLOGICAL DATA RECORDER received FDA 510(k) clearance under submission number K080375, sponsored by S.L.P. , Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Anesthesiology review panel. The statutory decision date of record is 2008-09-02.
- Submission: K080375
- Applicant / Sponsor: S.L.P. , Ltd.
- Clearance pathway: Traditional
- Review panel: Anesthesiology
- Device class: Class II
- Regulation citation: 21 CFR 868.2375
- Decision date: 2008-09-02
Classification & Regulation
This clearance is catalogued under FDA product code MNR and 21 CFR 868.2375, within the Anesthesiology review panel as a Class II device.