meddevicedb.com FDA Device Reference

SYNCHRON SYSTEMS AMMONIA REAGENT

K003196 Class I Traditional
Decision Date
2000-12-22
Sponsor / Applicant
Beckman Coulter, Inc.

Technical Specification

510(k) Submission ID K003196
Product Code JIF
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1065
Decision Date 2000-12-22
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SYNCHRON SYSTEMS AMMONIA REAGENT received FDA 510(k) clearance under submission number K003196, sponsored by Beckman Coulter, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Clinical Chemistry review panel. The statutory decision date of record is 2000-12-22.

Classification & Regulation

This clearance is catalogued under FDA product code JIF and 21 CFR 862.1065, within the Clinical Chemistry review panel as a Class I device.