meddevicedb.com FDA Device Reference

HEMESPEC CHECK SET

K800852 Class II Traditional
Decision Date
1980-05-02
Sponsor / Applicant
Helena Laboratories

Technical Specification

510(k) Submission ID K800852
Product Code KRZ
Medical Specialty / Panel Hematology
Regulation Citation 21 CFR 864.8165
Decision Date 1980-05-02
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

HEMESPEC CHECK SET received FDA 510(k) clearance under submission number K800852, sponsored by Helena Laboratories. The device was reviewed via the Traditional premarket notification pathway and assigned to the Hematology review panel. The statutory decision date of record is 1980-05-02.

Classification & Regulation

This clearance is catalogued under FDA product code KRZ and 21 CFR 864.8165, within the Hematology review panel as a Class II device.