510(k) Report

FDA applicant

Map Medizintechnik Fur Arzt Und Patient GmbH

Poway, CA3 decisions2000–20040 recalls

FDA records 3 decisions for Map Medizintechnik Fur Arzt Und Patient GmbH (Poway, CA) from 2000 to 2004: 3 510(k) clearances. Most are in product codes BZD (Ventilator, Non-Continuous (Respirator)) and MNR (Ventilatory Effort Recorder). Its devices cite 2 predicates, 0 of them its own earlier devices. 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, anesthesiology panel, where it files most

How often FDA has decided Map Medizintechnik Fur Arzt Und Patient GmbH’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Map Medizintechnik Fur Arzt Und Patient GmbH since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Map Medizintechnik Fur Arzt Und Patient GmbH by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Map Medizintechnik Fur Arzt Und…’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

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