Clearance Summary
PRESSURE MONITOR received FDA 510(k) clearance under submission number K842194, sponsored by Norton Texas Medical Products. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 1984-08-27.
- Submission: K842194
- Applicant / Sponsor: Norton Texas Medical Products
- Clearance pathway: Traditional
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.4310
- Decision date: 1984-08-27
Classification & Regulation
This clearance is catalogued under FDA product code DXS and 21 CFR 870.4310, within the Cardiovascular review panel as a Class II device.