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STREAMLINE AIRLESS SYSTEM SET WITH PRE-ATTACHED DIALYZER

K113023 Class II Traditional
Decision Date
2012-12-21
Sponsor / Applicant
Nxstage Medical, Inc.

Technical Specification

510(k) Submission ID K113023
Product Code KDI
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.5860
Decision Date 2012-12-21
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

STREAMLINE AIRLESS SYSTEM SET WITH PRE-ATTACHED DIALYZER received FDA 510(k) clearance under submission number K113023, sponsored by Nxstage Medical, Inc.. 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 2012-12-21.

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.