meddevicedb.com FDA Device Reference

HEMOGLOBIN ANALYZER & PERFORM. CHECK SET

K771101 Class II Traditional
Decision Date
1977-07-21
Sponsor / Applicant
The Dow Chemical Co.

Technical Specification

510(k) Submission ID K771101
Product Code GIG
Medical Specialty / Panel Hematology
Regulation Citation 21 CFR 864.7500
Decision Date 1977-07-21
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

HEMOGLOBIN ANALYZER & PERFORM. CHECK SET received FDA 510(k) clearance under submission number K771101, sponsored by The Dow Chemical Co.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Hematology review panel. The statutory decision date of record is 1977-07-21.

Classification & Regulation

This clearance is catalogued under FDA product code GIG and 21 CFR 864.7500, within the Hematology review panel as a Class II device.