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ALPHA INFUSION PUMP AND CATHETERS

K021964 Class II Traditional
Decision Date
2002-08-12
Sponsor / Applicant
Advanced Infusion, Inc.

Technical Specification

510(k) Submission ID K021964
Product Code MEB
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5725
Decision Date 2002-08-12
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ALPHA INFUSION PUMP AND CATHETERS received FDA 510(k) clearance under submission number K021964, sponsored by Advanced Infusion, 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 2002-08-12.

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.