meddevicedb.com FDA Device Reference

CAPILLARY GAS CHROMATOGRAPHIC COLUMNS

K841712 Class I Traditional
Decision Date
1984-05-21
Sponsor / Applicant
Supelco, Inc.

Technical Specification

510(k) Submission ID K841712
Product Code DII
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.2250
Decision Date 1984-05-21
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CAPILLARY GAS CHROMATOGRAPHIC COLUMNS received FDA 510(k) clearance under submission number K841712, sponsored by Supelco, 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 1984-05-21.

Classification & Regulation

This clearance is catalogued under FDA product code DII and 21 CFR 862.2250, within the Clinical Chemistry review panel as a Class I device.