meddevicedb.com FDA Device Reference

AFF (MARK I) VOLUMETRIC INFUSION PUMP

K070529 Class II Traditional
Decision Date
2007-05-08
Sponsor / Applicant
Definitive Medical Technologies, Ltd.

Technical Specification

510(k) Submission ID K070529
Product Code FRN
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5725
Decision Date 2007-05-08
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

AFF (MARK I) VOLUMETRIC INFUSION PUMP received FDA 510(k) clearance under submission number K070529, sponsored by Definitive Medical Technologies, Ltd.. 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 2007-05-08.

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.