meddevicedb.com FDA Device Reference

ACCUFLOW AND ACCUFLUX ELASTOMERIC INFUSION PUMP

K081905 Class II Traditional
Decision Date
2008-07-15
Sponsor / Applicant
Westmed, Inc.

Technical Specification

510(k) Submission ID K081905
Product Code MEB
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5725
Decision Date 2008-07-15
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ACCUFLOW AND ACCUFLUX ELASTOMERIC INFUSION PUMP received FDA 510(k) clearance under submission number K081905, sponsored by Westmed, 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 2008-07-15.

Classification & Regulation

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