meddevicedb.com FDA Device Reference

FREEDOM 60 SYRINGE INFUSION PUMP SYSTEM WITH SYRINGE SET & TUBING

K933652 Class II Traditional
Decision Date
1994-05-18
Sponsor / Applicant
Repro-Med Systems, Inc.

Technical Specification

510(k) Submission ID K933652
Product Code FRN
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5725
Decision Date 1994-05-18
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

FREEDOM 60 SYRINGE INFUSION PUMP SYSTEM WITH SYRINGE SET & TUBING received FDA 510(k) clearance under submission number K933652, sponsored by Repro-Med Systems, 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 1994-05-18.

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.