meddevicedb.com FDA Device Reference

PLATELET RETENTION (ADHESION) COLUMNS

K800037 Class II Traditional
Decision Date
1980-02-05
Sponsor / Applicant
Hemometrix

Technical Specification

510(k) Submission ID K800037
Product Code JBZ
Medical Specialty / Panel Hematology
Regulation Citation 21 CFR 864.6650
Decision Date 1980-02-05
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PLATELET RETENTION (ADHESION) COLUMNS received FDA 510(k) clearance under submission number K800037, sponsored by Hemometrix. The device was reviewed via the Traditional premarket notification pathway and assigned to the Hematology review panel. The statutory decision date of record is 1980-02-05.

Classification & Regulation

This clearance is catalogued under FDA product code JBZ and 21 CFR 864.6650, within the Hematology review panel as a Class II device.