meddevicedb.com FDA Device Reference

HOTLINE 2 FLUID WARMER

K001764 Class II Traditional
Decision Date
2000-08-09
Sponsor / Applicant
Sims Level 1, Inc.

Technical Specification

510(k) Submission ID K001764
Product Code LGZ
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5725
Decision Date 2000-08-09
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

HOTLINE 2 FLUID WARMER received FDA 510(k) clearance under submission number K001764, sponsored by Sims Level 1, 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 2000-08-09.

Classification & Regulation

This clearance is catalogued under FDA product code LGZ and 21 CFR 880.5725, within the General Hospital review panel as a Class II device.