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ALLIENT SORBET HEMODIALYSIS SYSTEM, MODEL 1100

K060381 Class II Special
Decision Date
2006-05-24
Sponsor / Applicant
Renal Solutions, Inc.

Technical Specification

510(k) Submission ID K060381
Product Code FKT
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.5600
Decision Date 2006-05-24
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ALLIENT SORBET HEMODIALYSIS SYSTEM, MODEL 1100 received FDA 510(k) clearance under submission number K060381, sponsored by Renal Solutions, Inc.. The device was reviewed via the Special premarket notification pathway and assigned to the Gastroenterology, Urology review panel. The statutory decision date of record is 2006-05-24.

Classification & Regulation

This clearance is catalogued under FDA product code FKT and 21 CFR 876.5600, within the Gastroenterology, Urology review panel as a Class II device.