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AMRESCO BUN-KINETIC REAGENTS PRODUCTS #7583

K900394 Class II Traditional
Decision Date
1990-04-11
Sponsor / Applicant
American Research Products Co.

Technical Specification

510(k) Submission ID K900394
Product Code CDQ
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1770
Decision Date 1990-04-11
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

AMRESCO BUN-KINETIC REAGENTS PRODUCTS #7583 received FDA 510(k) clearance under submission number K900394, sponsored by American Research Products Co.. 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 1990-04-11.

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.