meddevicedb.com FDA Device Reference

LABTRONIX PLATELET COUNTER(L/O/C.)

K811084 Class I Traditional
Decision Date
1981-07-23
Sponsor / Applicant
Labtronix Corp.

Technical Specification

510(k) Submission ID K811084
Product Code GLG
Medical Specialty / Panel Hematology
Regulation Citation 21 CFR 864.6160
Decision Date 1981-07-23
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

LABTRONIX PLATELET COUNTER(L/O/C.) received FDA 510(k) clearance under submission number K811084, sponsored by Labtronix Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Hematology review panel. The statutory decision date of record is 1981-07-23.

Classification & Regulation

This clearance is catalogued under FDA product code GLG and 21 CFR 864.6160, within the Hematology review panel as a Class I device.