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CLINISTAT DRY CHEM ANALYZER/URIC ACID REAGENT TEST

K883321 Class I Traditional
Decision Date
1988-10-25
Sponsor / Applicant
Heraeus Kulzer, Inc.

Technical Specification

510(k) Submission ID K883321
Product Code JJE
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.2160
Decision Date 1988-10-25
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CLINISTAT DRY CHEM ANALYZER/URIC ACID REAGENT TEST received FDA 510(k) clearance under submission number K883321, sponsored by Heraeus Kulzer, 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 1988-10-25.

Classification & Regulation

This clearance is catalogued under FDA product code JJE and 21 CFR 862.2160, within the Clinical Chemistry review panel as a Class I device.