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EXTRELUT QE EXTRACTION COLUMNS

K831027 Class I Traditional
Decision Date
1983-05-16
Sponsor / Applicant
Emd Chemicals, Inc.

Technical Specification

510(k) Submission ID K831027
Product Code KEA
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.2230
Decision Date 1983-05-16
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

EXTRELUT QE EXTRACTION COLUMNS received FDA 510(k) clearance under submission number K831027, sponsored by Emd Chemicals, 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 1983-05-16.

Classification & Regulation

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