meddevicedb.com FDA Device Reference

Micro Catheter

K202926 Class II Traditional
Decision Date
2022-02-10
Sponsor / Applicant
Shanghai Heartcare Medical Technology Co., Ltd.

Technical Specification

510(k) Submission ID K202926
Product Code QJP
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1250
Decision Date 2022-02-10
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Micro Catheter received FDA 510(k) clearance under submission number K202926, sponsored by Shanghai Heartcare Medical Technology Co., Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2022-02-10.

Classification & Regulation

This clearance is catalogued under FDA product code QJP and 21 CFR 870.1250, within the Cardiovascular review panel as a Class II device.