meddevicedb.com FDA Device Reference

CMS 2000 SERIES TPN KITS

K831964 Class I Traditional
Decision Date
1983-08-11
Sponsor / Applicant
Currie Medical Specialties, Inc.

Technical Specification

510(k) Submission ID K831964
Product Code FMC
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.6250
Decision Date 1983-08-11
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CMS 2000 SERIES TPN KITS received FDA 510(k) clearance under submission number K831964, sponsored by Currie Medical Specialties, 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 1983-08-11.

Classification & Regulation

This clearance is catalogued under FDA product code FMC and 21 CFR 880.6250, within the General Hospital review panel as a Class I device.