510(k) Report

FDA applicant

Mse Medizintechnik GmbH & Co. KG

Rodemark, DE1 decision1995–19950 recalls

FDA records 1 decision for Mse Medizintechnik GmbH & Co. KG (Rodemark, DE) in 1995: 1 510(k) clearance. All are in product code IYW (Scanner, Rectilinear, Nuclear). No recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, radiology panel, where it files most

How often FDA has decided Mse Medizintechnik GmbH & Co. KG’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Mse Medizintechnik GmbH & Co. KG since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Mse Medizintechnik GmbH & Co. KG by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Which product codes does it file in?

  • IYWScanner, Rectilinear, Nuclear1decision

What has FDA decided for it lately?

  • K944684Polyscan Digital ScannerMse Medizintechnik GmbH & Co. KG · 1995

The one decision as Mse Medizintechnik GmbH & Co. KG →