meddevicedb.com FDA Device Reference

LPC II

K812031 Class II Traditional
Decision Date
1981-08-12
Sponsor / Applicant
Labtronix Corp.

Technical Specification

510(k) Submission ID K812031
Product Code GKL
Medical Specialty / Panel Hematology
Regulation Citation 21 CFR 864.5200
Decision Date 1981-08-12
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

LPC II received FDA 510(k) clearance under submission number K812031, 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 1981-08-12.

Classification & Regulation

This clearance is catalogued under FDA product code GKL and 21 CFR 864.5200, within the Hematology review panel as a Class II device.