meddevicedb.com FDA Device Reference

LAKE REGION VARIABLE STIFFNESS GUIDEWIRE (VSGW)

K871882 Class II Traditional
Decision Date
1987-09-15
Sponsor / Applicant
Lake Region Mfg., Inc.

Technical Specification

510(k) Submission ID K871882
Product Code DQX
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1330
Decision Date 1987-09-15
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

LAKE REGION VARIABLE STIFFNESS GUIDEWIRE (VSGW) received FDA 510(k) clearance under submission number K871882, sponsored by Lake Region Mfg., 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 1987-09-15.

Classification & Regulation

This clearance is catalogued under FDA product code DQX and 21 CFR 870.1330, within the Cardiovascular review panel as a Class II device.