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3388 REPORTING INTEGRATOR

K792158 Class I Traditional
Decision Date
1979-11-16
Sponsor / Applicant
Hewlett-Packard Co.

Technical Specification

510(k) Submission ID K792158
Product Code JQP
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.2100
Decision Date 1979-11-16
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

3388 REPORTING INTEGRATOR received FDA 510(k) clearance under submission number K792158, 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 1979-11-16.

Classification & Regulation

This clearance is catalogued under FDA product code JQP and 21 CFR 862.2100, within the Clinical Chemistry review panel as a Class I device.