meddevicedb.com FDA Device Reference

Arterial Pressure Monitoring Set/Tray

K254278 Class II Special
Decision Date
2026-03-25
Sponsor / Applicant
Spectrum Vascular

Technical Specification

510(k) Submission ID K254278
Product Code DQO
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1200
Decision Date 2026-03-25
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Arterial Pressure Monitoring Set/Tray received FDA 510(k) clearance under submission number K254278, sponsored by Spectrum Vascular. The device was reviewed via the Special premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2026-03-25.

Classification & Regulation

This clearance is catalogued under FDA product code DQO and 21 CFR 870.1200, within the Cardiovascular review panel as a Class II device.