meddevicedb.com FDA Device Reference

PROMINJECT PROGRAMMABLE INFUSION PUMP

K850669 Class II Traditional
Decision Date
1985-04-09
Sponsor / Applicant
Pharmacia, Inc.

Technical Specification

510(k) Submission ID K850669
Product Code FRN
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5725
Decision Date 1985-04-09
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PROMINJECT PROGRAMMABLE INFUSION PUMP received FDA 510(k) clearance under submission number K850669, sponsored by Pharmacia, 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 1985-04-09.

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.