meddevicedb.com FDA Device Reference

3400 INFUSION PUMP

K931318 Class II Traditional
Decision Date
1994-12-09
Sponsor / Applicant
Graseby Medical , Ltd.

Technical Specification

510(k) Submission ID K931318
Product Code FRN
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5725
Decision Date 1994-12-09
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

3400 INFUSION PUMP received FDA 510(k) clearance under submission number K931318, sponsored by Graseby Medical , Ltd.. 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 1994-12-09.

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.