meddevicedb.com FDA Device Reference

AMBULATORY INFUSION PUMP DRUG RESERVOIR

K870524 Class II Traditional
Decision Date
1987-05-06
Sponsor / Applicant
Med Fusion Systems, Inc.

Technical Specification

510(k) Submission ID K870524
Product Code FRN
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5725
Decision Date 1987-05-06
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

AMBULATORY INFUSION PUMP DRUG RESERVOIR received FDA 510(k) clearance under submission number K870524, sponsored by Med Fusion Systems, 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 1987-05-06.

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.