MODIFICATION TO D-TRONPLUS— 510(k) K043000

Name: FDA 510(k) clearance K043000
Creator: U.S. Food and Drug Administration
Published: 2004-12-01

Substantially Equivalent

Disetronic Medical Systems AG

FDA 510(k) clearance K043000 for MODIFICATION TO D-TRONPLUS, Substantially Equivalent on 2004-12-01. Applicant: Disetronic Medical Systems AG. Device class: 2.

Clearance details

Applicant: Disetronic Medical Systems AG
Product code: Code LZG
Device class: Class 2
Regulation: 21 CFR 880.5725
Advisory panel: General Hospital
Date received: 2004-11-01
Decision date: 2004-12-01
Decision: Substantially Equivalent
Clearance type: Special
Location: Indianapolis, IN, US

Download summary PDF View on FDA.gov ↗

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Adverse events under product code LZG

product code LZG

Death: 104
Injury: 12,022
Malfunction: 135,004
Other: 1
Total: 147,131

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.