meddevicedb.com FDA Device Reference

BLOOD GAS & FLAME PHOTOMETER INSTRU-

K831075 Class I Traditional
Decision Date
1983-06-22
Sponsor / Applicant
United Diagnostics, Inc.

Technical Specification

510(k) Submission ID K831075
Product Code CGC
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1325
Decision Date 1983-06-22
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

BLOOD GAS & FLAME PHOTOMETER INSTRU- received FDA 510(k) clearance under submission number K831075, sponsored by United Diagnostics, 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 1983-06-22.

Classification & Regulation

This clearance is catalogued under FDA product code CGC and 21 CFR 862.1325, within the Clinical Chemistry review panel as a Class I device.