meddevicedb.com FDA Device Reference

MODEL AS* 7B AUTOSYRINGE INFUSION PUMP

K802166 Class II Traditional
Decision Date
1980-11-12
Sponsor / Applicant
Baxter Healthcare Corp

Technical Specification

510(k) Submission ID K802166
Product Code FLN
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.2420
Decision Date 1980-11-12
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MODEL AS* 7B AUTOSYRINGE INFUSION PUMP received FDA 510(k) clearance under submission number K802166, 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 1980-11-12.

Classification & Regulation

This clearance is catalogued under FDA product code FLN and 21 CFR 880.2420, within the General Hospital review panel as a Class II device.