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PREMIER HB9210 HBA1C ANALYZER

K112015 Class II Traditional
Decision Date
2011-11-22
Sponsor / Applicant
Primus Corporation Dba Trinity Biotech

Technical Specification

510(k) Submission ID K112015
Product Code LCP
Medical Specialty / Panel Hematology
Regulation Citation 21 CFR 864.7470
Decision Date 2011-11-22
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PREMIER HB9210 HBA1C ANALYZER received FDA 510(k) clearance under submission number K112015, sponsored by Primus Corporation Dba Trinity Biotech. The device was reviewed via the Traditional premarket notification pathway and assigned to the Hematology review panel. The statutory decision date of record is 2011-11-22.

Classification & Regulation

This clearance is catalogued under FDA product code LCP and 21 CFR 864.7470, within the Hematology review panel as a Class II device.