meddevicedb.com FDA Device Reference

SYSTEMATE URIC ACID (URCA) ITEM NUMBER 65422

K903335 Class I Traditional
Decision Date
1990-08-17
Sponsor / Applicant
Em Diagnostic Systems, Inc.

Technical Specification

510(k) Submission ID K903335
Product Code CDO
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1775
Decision Date 1990-08-17
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SYSTEMATE URIC ACID (URCA) ITEM NUMBER 65422 received FDA 510(k) clearance under submission number K903335, sponsored by Em Diagnostic Systems, 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 1990-08-17.

Classification & Regulation

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