meddevicedb.com FDA Device Reference

ION 2 REAGENT KI

K851350 Class II Traditional
Decision Date
1985-04-29
Sponsor / Applicant
Hi Chem, Inc.

Technical Specification

510(k) Submission ID K851350
Product Code CEM
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1600
Decision Date 1985-04-29
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ION 2 REAGENT KI received FDA 510(k) clearance under submission number K851350, sponsored by Hi Chem, 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 1985-04-29.

Classification & Regulation

This clearance is catalogued under FDA product code CEM and 21 CFR 862.1600, within the Clinical Chemistry review panel as a Class II device.