FDA applicant

Magnetic Resonance Equipment Corp.

Bay Shore, NY5 decisions1993–20011 recall

FDA records 5 decisions for Magnetic Resonance Equipment Corp. (Bay Shore, NY) from 1993 to 2001: 5 510(k) clearances. Most are in product codes DQA (Oximeter) and CCK (Analyzer, Gas, Carbon-Dioxide, Gaseous-Phase). 1 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, cardiovascular panel, where it files most

How often FDA has decided Magnetic Resonance Equipment Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Magnetic Resonance Equipment Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Magnetic Resonance Equipment Corp. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Other applicant names beginning “Magnetic”

FDA records each applicant name separately; these may or may not be the same firm.

Magnetic Research, Inc. 9 Magnetic Resonance Plus, Inc. 1 Magnetic Moments, LLC 1

Magnetic Resonance Equipment Corp.

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

What has been recalled?

Other applicant names beginning “Magnetic”