meddevicedb.com FDA Device Reference

INORGANIC PHOSPHOROUS FOR DEMAND ANALYZER

K850380 Class I Traditional
Decision Date
1985-03-01
Sponsor / Applicant
Advanced Biomedical Methods, Inc.

Technical Specification

510(k) Submission ID K850380
Product Code CEO
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1580
Decision Date 1985-03-01
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

INORGANIC PHOSPHOROUS FOR DEMAND ANALYZER received FDA 510(k) clearance under submission number K850380, sponsored by Advanced Biomedical Methods, 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 1985-03-01.

Classification & Regulation

This clearance is catalogued under FDA product code CEO and 21 CFR 862.1580, within the Clinical Chemistry review panel as a Class I device.