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PHOSPHOTUNGSTATE REDUCTION, URIC ACID

K813076 Class I Traditional
Decision Date
1981-11-16
Sponsor / Applicant
American Monitor Corp.

Technical Specification

510(k) Submission ID K813076
Product Code CDH
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1775
Decision Date 1981-11-16
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PHOSPHOTUNGSTATE REDUCTION, URIC ACID received FDA 510(k) clearance under submission number K813076, sponsored by American Monitor 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 1981-11-16.

Classification & Regulation

This clearance is catalogued under FDA product code CDH and 21 CFR 862.1775, within the Clinical Chemistry review panel as a Class I device.