meddevicedb.com FDA Device Reference

Cardiovascular Angiography System

K220311 Class II Traditional
Decision Date
2022-05-03
Sponsor / Applicant
Allengers Medical Systems Limited

Technical Specification

510(k) Submission ID K220311
Product Code OWB
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1650
Decision Date 2022-05-03
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Cardiovascular Angiography System received FDA 510(k) clearance under submission number K220311, sponsored by Allengers Medical Systems Limited. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2022-05-03.

Classification & Regulation

This clearance is catalogued under FDA product code OWB and 21 CFR 892.1650, within the Radiology review panel as a Class II device.