meddevicedb.com FDA Device Reference

BOND ELUT COLUMNS

K800061 Class I Traditional
Decision Date
1980-03-12
Sponsor / Applicant
Analytichem International, Inc.

Technical Specification

510(k) Submission ID K800061
Product Code DJY
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.2230
Decision Date 1980-03-12
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

BOND ELUT COLUMNS received FDA 510(k) clearance under submission number K800061, sponsored by Analytichem International, 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 1980-03-12.

Classification & Regulation

This clearance is catalogued under FDA product code DJY and 21 CFR 862.2230, within the Clinical Chemistry review panel as a Class I device.