meddevicedb.com FDA Device Reference

IDS-ISYS 25-HYDROXY VITAMIN D ASSAY, IDS-ISYS 25-HYDROXY VITAMIN D CONTROL SET

K091849 Class II Traditional
Decision Date
2010-06-25
Sponsor / Applicant
Immunodiagnostic Systems, Inc.

Technical Specification

510(k) Submission ID K091849
Product Code MRG
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1825
Decision Date 2010-06-25
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

IDS-ISYS 25-HYDROXY VITAMIN D ASSAY, IDS-ISYS 25-HYDROXY VITAMIN D CONTROL SET received FDA 510(k) clearance under submission number K091849, sponsored by Immunodiagnostic Systems, Inc.. 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 2010-06-25.

Classification & Regulation

This clearance is catalogued under FDA product code MRG and 21 CFR 862.1825, within the Clinical Chemistry review panel as a Class II device.