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NXSTAGE EXPRESS FLUID WARMER

K140623 Class II Special
Decision Date
2014-06-16
Sponsor / Applicant
Nxstage Medical, Inc.

Technical Specification

510(k) Submission ID K140623
Product Code FLA
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.5820
Decision Date 2014-06-16
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

NXSTAGE EXPRESS FLUID WARMER received FDA 510(k) clearance under submission number K140623, sponsored by Nxstage Medical, 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 2014-06-16.

Classification & Regulation

This clearance is catalogued under FDA product code FLA and 21 CFR 876.5820, within the Gastroenterology, Urology review panel as a Class II device.