meddevicedb.com FDA Device Reference

Normal Saline Flush

K150143 Class II Traditional
Decision Date
2015-08-31
Sponsor / Applicant
Nurse Assist, Inc.

Technical Specification

510(k) Submission ID K150143
Product Code NGT
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5200
Decision Date 2015-08-31
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Normal Saline Flush received FDA 510(k) clearance under submission number K150143, sponsored by Nurse Assist, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the General Hospital review panel. The statutory decision date of record is 2015-08-31.

Classification & Regulation

This clearance is catalogued under FDA product code NGT and 21 CFR 880.5200, within the General Hospital review panel as a Class II device.