meddevicedb.com FDA Device Reference

ANALYTE CARBON DIOXIDE ASSAYED ON TECHNICON RA(TM)

K880609 Class II Traditional
Decision Date
1988-03-16
Sponsor / Applicant
Technicon Instruments Corp.

Technical Specification

510(k) Submission ID K880609
Product Code KHS
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1160
Decision Date 1988-03-16
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ANALYTE CARBON DIOXIDE ASSAYED ON TECHNICON RA(TM) received FDA 510(k) clearance under submission number K880609, sponsored by Technicon Instruments 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 1988-03-16.

Classification & Regulation

This clearance is catalogued under FDA product code KHS and 21 CFR 862.1160, within the Clinical Chemistry review panel as a Class II device.