meddevicedb.com FDA Device Reference

WATERS 460 LIQUID CHROMATOGRAPHY ELECTROCHEMICAL D

K850359 Class I Traditional
Decision Date
1985-03-05
Sponsor / Applicant
Millipore Corp.

Technical Specification

510(k) Submission ID K850359
Product Code LDM
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.2260
Decision Date 1985-03-05
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

WATERS 460 LIQUID CHROMATOGRAPHY ELECTROCHEMICAL D received FDA 510(k) clearance under submission number K850359, sponsored by Millipore Corp.. 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 1985-03-05.

Classification & Regulation

This clearance is catalogued under FDA product code LDM and 21 CFR 862.2260, within the Clinical Chemistry review panel as a Class I device.