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FRESENIUS RENAL ACUTE CARE (RAC 100) FILTER, MODEL 0500610N

K070222 Class II Traditional
Decision Date
2007-04-24
Sponsor / Applicant
Fresenius Medical Care North America

Technical Specification

510(k) Submission ID K070222
Product Code KDI
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.5860
Decision Date 2007-04-24
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

FRESENIUS RENAL ACUTE CARE (RAC 100) FILTER, MODEL 0500610N received FDA 510(k) clearance under submission number K070222, sponsored by Fresenius Medical Care North America. 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 2007-04-24.

Classification & Regulation

This clearance is catalogued under FDA product code KDI and 21 CFR 876.5860, within the Gastroenterology, Urology review panel as a Class II device.