FDA applicant

Litton Medical Systems

Mchenry, IL8 decisions1976–19770 recalls

FDA records 8 decisions for Litton Medical Systems (Mchenry, IL) from 1976 to 1977: 8 510(k) clearances. Most are in product codes IZO (Generator, High-Voltage, X-Ray, Diagnostic) and JAA (System, X-Ray, Fluoroscopic, Image-Intensified). 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, radiology panel, where it files most

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

FDA decisions per year

No FDA decision for Litton Medical Systems since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Litton Medical Systems 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 Medical Electronics 38 Litton Bionetics 15 Litton Dental Products 12 Litton Datamedix 5 Litton Systems, Inc. 4

Litton Medical Systems

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Litton”