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EASYRA MG REAGENT, MODEL 10220

K092737 Class I Special
Decision Date
2009-11-17
Sponsor / Applicant
Medica Corp.

Technical Specification

510(k) Submission ID K092737
Product Code JGJ
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1495
Decision Date 2009-11-17
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

EASYRA MG REAGENT, MODEL 10220 received FDA 510(k) clearance under submission number K092737, sponsored by Medica Corp.. The device was reviewed via the Special premarket notification pathway and assigned to the Clinical Chemistry review panel. The statutory decision date of record is 2009-11-17.

Classification & Regulation

This clearance is catalogued under FDA product code JGJ and 21 CFR 862.1495, within the Clinical Chemistry review panel as a Class I device.