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EASYRA UREA NITROGEN AND CREATININE REAGENTS

K110675 Class II Traditional
Decision Date
2011-04-21
Sponsor / Applicant
Medica Corp.

Technical Specification

510(k) Submission ID K110675
Product Code CDQ
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1770
Decision Date 2011-04-21
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

EASYRA UREA NITROGEN AND CREATININE REAGENTS received FDA 510(k) clearance under submission number K110675, sponsored by Medica 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 2011-04-21.

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.