510(k) Report

FDA applicant

Medical Instruments Corporation Mic AG

Solothurn, CH2 decisions1996–19990 recalls

FDA records 2 decisions for Medical Instruments Corporation Mic AG (Solothurn, CH) from 1996 to 1999: 2 510(k) clearances. Most are in product codes LYR (Helicobacter Pylori) and FFT (Electrode, Ph, Stomach). 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, microbiology panel, where it files most

How often FDA has decided Medical Instruments Corporation Mic AG’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Medical Instruments Corporation Mic AG since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Medical Instruments Corporation Mic AG 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?

  • LYRHelicobacter Pylori1decision
  • FFTElectrode, Ph, Stomach1decision

What has FDA decided for it lately?

  • K991248Pronto DryMedical Instruments Corporation Mic AG · 1999
  • K950087LOT 440Medical Instruments Corporation Mic AG · 1996

All 2 as Medical Instruments Corporation Mic AG →