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BUN TEST UNI-UV BLOOD UREA NITROGEN TEST

K780943 Class II Traditional
Decision Date
1978-07-27
Sponsor / Applicant
Sclavo, Inc.

Technical Specification

510(k) Submission ID K780943
Product Code CDQ
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1770
Decision Date 1978-07-27
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

BUN TEST UNI-UV BLOOD UREA NITROGEN TEST received FDA 510(k) clearance under submission number K780943, 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 1978-07-27.

Classification & Regulation

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