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ACTIM PROM AND CONTROLS

K061886 Class I Traditional
Decision Date
2007-01-25
Sponsor / Applicant
Medix Biochemica

Technical Specification

510(k) Submission ID K061886
Product Code OAM
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1550
Decision Date 2007-01-25
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ACTIM PROM AND CONTROLS received FDA 510(k) clearance under submission number K061886, sponsored by Medix Biochemica. 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 2007-01-25.

Classification & Regulation

This clearance is catalogued under FDA product code OAM and 21 CFR 862.1550, within the Clinical Chemistry review panel as a Class I device.