meddevicedb.com FDA Device Reference

MIRA-FLEX 18 MICROCATHETER

K052841 Class II Special
Decision Date
2005-12-08
Sponsor / Applicant
Cook, Inc.

Technical Specification

510(k) Submission ID K052841
Product Code KRA
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1210
Decision Date 2005-12-08
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MIRA-FLEX 18 MICROCATHETER received FDA 510(k) clearance under submission number K052841, sponsored by Cook, Inc.. The device was reviewed via the Special premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2005-12-08.

Classification & Regulation

This clearance is catalogued under FDA product code KRA and 21 CFR 870.1210, within the Cardiovascular review panel as a Class II device.