meddevicedb.com FDA Device Reference

Lubricity

K163476 Traditional
Decision Date
2017-05-10
Sponsor / Applicant
You First Services, Incorporated

Technical Specification

510(k) Submission ID K163476
Product Code LFD
Medical Specialty / Panel Unknown
Decision Date 2017-05-10
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Lubricity received FDA 510(k) clearance under submission number K163476, sponsored by You First Services, Incorporated. The device was reviewed via the Traditional premarket notification pathway and assigned to the Unknown review panel. The statutory decision date of record is 2017-05-10.

Classification & Regulation

This clearance is catalogued under FDA product code LFD , within the Unknown review panel as a device.