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BUN REAGENT ASTRA 4 & 8 ANALYZERS

K802518 Class II Traditional
Decision Date
1980-11-12
Sponsor / Applicant
Nobel Scientific Industries, Inc.

Technical Specification

510(k) Submission ID K802518
Product Code CDN
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1770
Decision Date 1980-11-12
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

BUN REAGENT ASTRA 4 & 8 ANALYZERS received FDA 510(k) clearance under submission number K802518, sponsored by Nobel Scientific Industries, 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 1980-11-12.

Classification & Regulation

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