meddevicedb.com FDA Device Reference

GLUCOCARE INTENSIVE GLYCEMIC CONTROL SYSTEM

K081388 Class II Traditional
Decision Date
2008-08-21
Sponsor / Applicant
Pronia Medical System, LLC

Technical Specification

510(k) Submission ID K081388
Product Code NDC
Medical Specialty / Panel Anesthesiology
Regulation Citation 21 CFR 868.1890
Decision Date 2008-08-21
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

GLUCOCARE INTENSIVE GLYCEMIC CONTROL SYSTEM received FDA 510(k) clearance under submission number K081388, sponsored by Pronia Medical System, LLC. The device was reviewed via the Traditional premarket notification pathway and assigned to the Anesthesiology review panel. The statutory decision date of record is 2008-08-21.

Classification & Regulation

This clearance is catalogued under FDA product code NDC and 21 CFR 868.1890, within the Anesthesiology review panel as a Class II device.