meddevicedb.com FDA Device Reference

TERUFUSION INFUSION PUMP MODEL STC-502

K812339 Class II Traditional
Decision Date
1981-09-09
Sponsor / Applicant
Terumo Medical Corp.

Technical Specification

510(k) Submission ID K812339
Product Code FRN
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5725
Decision Date 1981-09-09
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

TERUFUSION INFUSION PUMP MODEL STC-502 received FDA 510(k) clearance under submission number K812339, sponsored by Terumo Medical Corp.. 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 1981-09-09.

Classification & Regulation

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