meddevicedb.com FDA Device Reference

PLT-4 SIZE-CHECK

K802267 Class II Traditional
Decision Date
1980-11-12
Sponsor / Applicant
R&D Systems, Inc.

Technical Specification

510(k) Submission ID K802267
Product Code JPK
Medical Specialty / Panel Hematology
Regulation Citation 21 CFR 864.8625
Decision Date 1980-11-12
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PLT-4 SIZE-CHECK received FDA 510(k) clearance under submission number K802267, sponsored by R&D Systems, 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 1980-11-12.

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.