meddevicedb.com FDA Device Reference

WIENER LAB. CALIBRATOR A PLUS, MODEL 2X3 ML CAT. NR. 1918006

K024305 Class II Traditional
Decision Date
2003-03-18
Sponsor / Applicant
Wiener Laboratories Saic

Technical Specification

510(k) Submission ID K024305
Product Code JIX
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1150
Decision Date 2003-03-18
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

WIENER LAB. CALIBRATOR A PLUS, MODEL 2X3 ML CAT. NR. 1918006 received FDA 510(k) clearance under submission number K024305, sponsored by Wiener Laboratories Saic. 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 2003-03-18.

Classification & Regulation

This clearance is catalogued under FDA product code JIX and 21 CFR 862.1150, within the Clinical Chemistry review panel as a Class II device.