FDA applicant

Litton Medical Electronics

Mchenry, IL38 decisions1982–19850 recalls

FDA records 38 decisions for Litton Medical Electronics (Mchenry, IL) from 1982 to 1985: 38 510(k) clearances. Most are in product codes DRT (Monitor, Cardiac (Incl. Cardiotachometer &…) and DPS (Electrocardiograph). 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, cardiovascular panel, where it files most

How often FDA has decided Litton Medical Electronics’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Litton Medical Electronics since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Litton Medical Electronics by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Other applicant names beginning “Litton”

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

Litton Bionetics 15 Litton Dental Products 12 Litton Medical Systems 8 Litton Datamedix 5 Litton Systems, Inc. 4

Litton Medical Electronics

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?

Other applicant names beginning “Litton”