meddevicedb.com FDA Device Reference

MSI-HC HEMATOLOGY CONTROL

K834043 Class II Traditional
Decision Date
1984-01-03
Sponsor / Applicant
Medical Specialties, Inc.

Technical Specification

510(k) Submission ID K834043
Product Code JPK
Medical Specialty / Panel Hematology
Regulation Citation 21 CFR 864.8625
Decision Date 1984-01-03
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MSI-HC HEMATOLOGY CONTROL received FDA 510(k) clearance under submission number K834043, sponsored by Medical Specialties, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Hematology review panel. The statutory decision date of record is 1984-01-03.

Classification & Regulation

This clearance is catalogued under FDA product code JPK and 21 CFR 864.8625, within the Hematology review panel as a Class II device.