meddevicedb.com FDA Device Reference

BUN-COLOR 2, BLOOD UREA NITROGEN TEST

K800902 Class II Traditional
Decision Date
1980-06-09
Sponsor / Applicant
Sclavo, Inc.

Technical Specification

510(k) Submission ID K800902
Product Code CDL
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1770
Decision Date 1980-06-09
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

BUN-COLOR 2, BLOOD UREA NITROGEN TEST received FDA 510(k) clearance under submission number K800902, sponsored by Sclavo, 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 1980-06-09.

Classification & Regulation

This clearance is catalogued under FDA product code CDL and 21 CFR 862.1770, within the Clinical Chemistry review panel as a Class II device.