meddevicedb.com FDA Device Reference

GAS-CHROMATOGRAPHIC PACKING

K801833 Class I Traditional
Decision Date
1980-08-27
Sponsor / Applicant
Supelco, Inc.

Technical Specification

510(k) Submission ID K801833
Product Code DJA
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.2250
Decision Date 1980-08-27
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

GAS-CHROMATOGRAPHIC PACKING received FDA 510(k) clearance under submission number K801833, 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 1980-08-27.

Classification & Regulation

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