FDA applicant

Rlt Medical Assoc., Inc.

Timonium, MD3 decisions1992–19990 recalls

FDA records 3 decisions for Rlt Medical Assoc., Inc. (Timonium, MD) from 1992 to 1999: 3 510(k) clearances. All are in product code DXH (Transmitters And Receivers…). Its devices cite 1 predicate, 1 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, cardiovascular panel, where it files most

How often FDA has decided Rlt Medical Assoc., Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Rlt Medical Assoc., Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Rlt Medical Assoc., Inc.

Which product codes does it file in?

Which of its devices are cited most?

What has FDA decided for it lately?