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EASYRA MICRO-ALBUMIN REAGENT AND CALIBRATOR

K101089 Class II Traditional
Decision Date
2011-07-13
Sponsor / Applicant
Medica Corp.

Technical Specification

510(k) Submission ID K101089
Product Code DCF
Medical Specialty / Panel Immunology
Regulation Citation 21 CFR 866.5040
Decision Date 2011-07-13
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

EASYRA MICRO-ALBUMIN REAGENT AND CALIBRATOR received FDA 510(k) clearance under submission number K101089, sponsored by Medica Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Immunology review panel. The statutory decision date of record is 2011-07-13.

Classification & Regulation

This clearance is catalogued under FDA product code DCF and 21 CFR 866.5040, within the Immunology review panel as a Class II device.