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LIBERTY PDX CYCLER

K141145 Class II Traditional
Decision Date
2014-07-30
Sponsor / Applicant
Fresenius Medical Care Renal Therapies Group, LLC

Technical Specification

510(k) Submission ID K141145
Product Code FKX
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.5630
Decision Date 2014-07-30
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

LIBERTY PDX CYCLER received FDA 510(k) clearance under submission number K141145, sponsored by Fresenius Medical Care Renal Therapies Group, LLC. The device was reviewed via the Traditional premarket notification pathway and assigned to the Gastroenterology, Urology review panel. The statutory decision date of record is 2014-07-30.

Classification & Regulation

This clearance is catalogued under FDA product code FKX and 21 CFR 876.5630, within the Gastroenterology, Urology review panel as a Class II device.