meddevicedb.com FDA Device Reference

MCC URICHECK ASSAYED LIQUID URINE MULTICONSTITUENT CONTROL

K012243 Class I Traditional
Decision Date
2001-08-20
Sponsor / Applicant
Hematronix, Inc.

Technical Specification

510(k) Submission ID K012243
Product Code JJY
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1660
Decision Date 2001-08-20
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MCC URICHECK ASSAYED LIQUID URINE MULTICONSTITUENT CONTROL received FDA 510(k) clearance under submission number K012243, sponsored by Hematronix, 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 2001-08-20.

Classification & Regulation

This clearance is catalogued under FDA product code JJY and 21 CFR 862.1660, within the Clinical Chemistry review panel as a Class I device.