FDA applicant

Dejarnette Research Systems

Towson, MD9 decisions1993–19980 recalls

FDA records 9 decisions for Dejarnette Research Systems (Towson, MD) from 1993 to 1998: 9 510(k) clearances. Most are in product codes LMD (System, Digital Image Communications…) and LMC (Camera, Multi Format, Radiological). 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 Dejarnette Research Systems’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Dejarnette Research Systems since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Dejarnette Research Systems

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?