meddevicedb.com FDA Device Reference

IVAC 280 VOLUMETRIC INFUSION CONTROLLER

K842419 Class II Traditional
Decision Date
1984-08-07
Sponsor / Applicant
Y

Technical Specification

510(k) Submission ID K842419
Product Code LDR
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5725
Decision Date 1984-08-07
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

IVAC 280 VOLUMETRIC INFUSION CONTROLLER received FDA 510(k) clearance under submission number K842419, sponsored by Y. 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 1984-08-07.

Classification & Regulation

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