meddevicedb.com FDA Device Reference

MODEL 304-S EXTERNAL MICRO-VOLUME INFUSION PUMP

K864327 Class I Traditional
Decision Date
1987-02-06
Sponsor / Applicant
Medtronic Minimed

Technical Specification

510(k) Submission ID K864327
Product Code FRW
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.2720
Decision Date 1987-02-06
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MODEL 304-S EXTERNAL MICRO-VOLUME INFUSION PUMP received FDA 510(k) clearance under submission number K864327, sponsored by Medtronic Minimed. 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 1987-02-06.

Classification & Regulation

This clearance is catalogued under FDA product code FRW and 21 CFR 880.2720, within the General Hospital review panel as a Class I device.