meddevicedb.com FDA Device Reference

EN-SNARE ENDOVASCULAR SNARE AND CATHETER

K021606 Class II Traditional
Decision Date
2002-05-31
Sponsor / Applicant
Medical Device Technologies, Inc.

Technical Specification

510(k) Submission ID K021606
Product Code MMX
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.5150
Decision Date 2002-05-31
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

EN-SNARE ENDOVASCULAR SNARE AND CATHETER received FDA 510(k) clearance under submission number K021606, sponsored by Medical Device Technologies, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2002-05-31.

Classification & Regulation

This clearance is catalogued under FDA product code MMX and 21 CFR 870.5150, within the Cardiovascular review panel as a Class II device.