meddevicedb.com FDA Device Reference

19091-XXXXX SER. OF GLASS CAPILLARY COL.

K791893 Class I Traditional
Decision Date
1979-10-30
Sponsor / Applicant
Hewlett-Packard Co.

Technical Specification

510(k) Submission ID K791893
Product Code DII
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.2250
Decision Date 1979-10-30
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

19091-XXXXX SER. OF GLASS CAPILLARY COL. received FDA 510(k) clearance under submission number K791893, 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 1979-10-30.

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.