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INFUSOR SV, INFUSOR LV, BAXTER PAIN MANAGEMENT SYSTEM

K002380 Class II Traditional
Decision Date
2000-09-05
Sponsor / Applicant
Baxter Healthcare Corp

Technical Specification

510(k) Submission ID K002380
Product Code FRN
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5725
Decision Date 2000-09-05
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

INFUSOR SV, INFUSOR LV, BAXTER PAIN MANAGEMENT SYSTEM received FDA 510(k) clearance under submission number K002380, 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 2000-09-05.

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.