meddevicedb.com FDA Device Reference

B-GCG SYSTEM BY RIA

K830526 Class II Traditional
Decision Date
1983-04-05
Sponsor / Applicant
Pcl-Ria, Inc.

Technical Specification

510(k) Submission ID K830526
Product Code JHI
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1155
Decision Date 1983-04-05
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

B-GCG SYSTEM BY RIA received FDA 510(k) clearance under submission number K830526, sponsored by Pcl-Ria, 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 1983-04-05.

Classification & Regulation

This clearance is catalogued under FDA product code JHI and 21 CFR 862.1155, within the Clinical Chemistry review panel as a Class II device.