Clearance Summary
ARTRAC VITAL SIGNS MON. MODELS 7000 AND 5000 & ACC received FDA 510(k) clearance under submission number K904088, sponsored by Sentinel. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 1991-02-05.
- Submission: K904088
- Applicant / Sponsor: Sentinel
- Clearance pathway: Traditional
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.2700
- Decision date: 1991-02-05
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.