FDA applicant

Mitsubishi Cable America, Inc.

Villa Park, CA3 decisions1994–19960 recalls

FDA records 3 decisions for Mitsubishi Cable America, Inc. (Villa Park, CA) from 1994 to 1996: 3 510(k) clearances. Most are in product codes EOB (Nasopharyngoscope (Flexible Or Rigid)) and FCQ (Light Source, Incandescent, Diagnostic). 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, gastroenterology and urology panel, where it files most

How often FDA has decided Mitsubishi Cable America, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Mitsubishi Cable America, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Mitsubishi Cable America, Inc. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Mitsubishi Cable America, Inc.’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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Other applicant names beginning “Mitsubishi”

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

Mitsubishi Intl. Corp. 5 Mitsubishi Kagaku Iatron 4 Mitsubishi Heavy Industries, Ltd. 3 Mitsubishi Electronics America, Inc. 3 Mitsubishi Chemical Medience Corporation 3 Mitsubishi Yuka America, Inc. 2 Mitsubishi Electric Corporation Kyoto Works 1

Mitsubishi Cable America, Inc.

Which product codes does it file in?

Whose devices does it build on?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Mitsubishi”