FORMOSTAR— 510(k) K862106

Name: FDA 510(k) clearance K862106
Creator: U.S. Food and Drug Administration
Published: 1986-08-21

Substantially Equivalent

Lmv, Liske & Methling, GmbH

FDA 510(k) clearance K862106 for FORMOSTAR, Substantially Equivalent on 1986-08-21. Applicant: Lmv, Liske & Methling, GmbH. Device class: 2.

Clearance details

Applicant: Lmv, Liske & Methling, GmbH
Product code: Code IRT
Device class: Class 2
Regulation: 21 CFR 890.5740
Advisory panel: Physical Medicine
Date received: 1986-06-02
Decision date: 1986-08-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Hamburg 76, W.-Germany, DE

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Recent devices under product code IRT

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Adverse events under product code IRT

product code IRT

Injury: 668
Total: 668

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.