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MODIFICATION TO DISETRONIC D-TRONPLUS INSULIN INFUSION PUMP

K022831 Class II Special
Decision Date
2002-09-11
Sponsor / Applicant
Disetronic Medical Systems AG

Technical Specification

510(k) Submission ID K022831
Product Code LZG
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5725
Decision Date 2002-09-11
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MODIFICATION TO DISETRONIC D-TRONPLUS INSULIN INFUSION PUMP received FDA 510(k) clearance under submission number K022831, sponsored by Disetronic Medical Systems AG. The device was reviewed via the Special premarket notification pathway and assigned to the General Hospital review panel. The statutory decision date of record is 2002-09-11.

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.