meddevicedb.com FDA Device Reference

I-FLOW ELASTOMERIC PUMP (ON-Q, PAINBUSTER, C-BLOC, HOMEPUMP)

K040337 Class II Traditional
Decision Date
2004-05-24
Sponsor / Applicant
I-Flow Corp.

Technical Specification

510(k) Submission ID K040337
Product Code MEB
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5725
Decision Date 2004-05-24
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

I-FLOW ELASTOMERIC PUMP (ON-Q, PAINBUSTER, C-BLOC, HOMEPUMP) received FDA 510(k) clearance under submission number K040337, sponsored by I-Flow Corp.. 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 2004-05-24.

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.