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Hematocrit and Metabolite QUALICHECK

K150226 Class I Traditional
Decision Date
2015-05-13
Sponsor / Applicant
Radiometer Medical Aps

Technical Specification

510(k) Submission ID K150226
Product Code JJS
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1660
Decision Date 2015-05-13
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Hematocrit and Metabolite QUALICHECK received FDA 510(k) clearance under submission number K150226, sponsored by Radiometer Medical Aps. 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 2015-05-13.

Classification & Regulation

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