meddevicedb.com FDA Device Reference

5880 SERIES OF GAS CHROMATOGRAPHS

K791138 Class I Traditional
Decision Date
1979-07-24
Sponsor / Applicant
Hewlett-Packard Co.

Technical Specification

510(k) Submission ID K791138
Product Code KZQ
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.2250
Decision Date 1979-07-24
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

5880 SERIES OF GAS CHROMATOGRAPHS received FDA 510(k) clearance under submission number K791138, sponsored by Hewlett-Packard Co.. 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 1979-07-24.

Classification & Regulation

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