FDA applicant

Rmp Co.

Fayetteville, NC4 decisions1983–19980 recalls

FDA records 4 decisions for Rmp Co. (Fayetteville, NC) from 1983 to 1998: 4 510(k) clearances. Most are in product codes HCC (Device, Biofeedback) and BZN (Cart, Emergency, Cardiopulmonary (Excluding…). No recall is linked to its devices.

FDA’s records also spell it “Rmp, Inc.”.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, neurology panel, where it files most

How often FDA has decided Rmp Co.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Rmp Co. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Rmp Co.

Which product codes does it file in?

What has FDA decided for it lately?