meddevicedb.com FDA Device Reference

HEMOGLOBIN CONTROL LEVELS

K801268 Class II Traditional
Decision Date
1980-07-14
Sponsor / Applicant
Bioscientific

Technical Specification

510(k) Submission ID K801268
Product Code KHG
Medical Specialty / Panel Hematology
Regulation Citation 21 CFR 864.7500
Decision Date 1980-07-14
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

HEMOGLOBIN CONTROL LEVELS received FDA 510(k) clearance under submission number K801268, sponsored by Bioscientific. The device was reviewed via the Traditional premarket notification pathway and assigned to the Hematology review panel. The statutory decision date of record is 1980-07-14.

Classification & Regulation

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