meddevicedb.com FDA Device Reference

UIBC FOR DISCREET RANDOM ACCESS ANALYZER

K932871 Class I Traditional
Decision Date
1993-09-08
Sponsor / Applicant
Catachem, Inc.

Technical Specification

510(k) Submission ID K932871
Product Code CFM
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1410
Decision Date 1993-09-08
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

UIBC FOR DISCREET RANDOM ACCESS ANALYZER received FDA 510(k) clearance under submission number K932871, sponsored by Catachem, 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 1993-09-08.

Classification & Regulation

This clearance is catalogued under FDA product code CFM and 21 CFR 862.1410, within the Clinical Chemistry review panel as a Class I device.