meddevicedb.com FDA Device Reference

PEARL DIABETES MANAGEMENT SYSTEM

K100567 Class II Traditional
Decision Date
2011-05-10
Sponsor / Applicant
M2 Group Holdings, Inc.

Technical Specification

510(k) Submission ID K100567
Product Code LZG
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5725
Decision Date 2011-05-10
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PEARL DIABETES MANAGEMENT SYSTEM received FDA 510(k) clearance under submission number K100567, sponsored by M2 Group Holdings, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the General Hospital review panel. The statutory decision date of record is 2011-05-10.

Classification & Regulation

This clearance is catalogued under FDA product code LZG and 21 CFR 880.5725, within the General Hospital review panel as a Class II device.