meddevicedb.com FDA Device Reference

MODEL AS6B INFUSION PUMP

K813590 Class II Traditional
Decision Date
1982-01-28
Sponsor / Applicant
Baxter Healthcare Corp

Technical Specification

510(k) Submission ID K813590
Product Code FRN
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5725
Decision Date 1982-01-28
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MODEL AS6B INFUSION PUMP received FDA 510(k) clearance under submission number K813590, sponsored by Baxter Healthcare 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 1982-01-28.

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.