510(k) Report

FDA applicant

Neurim Pharmaceuticals, Ltd.

Rockville, MD1 decision1997–19970 recalls

FDA records 1 decision for Neurim Pharmaceuticals, Ltd. (Rockville, MD) in 1997: 1 510(k) clearance. All are in product code LEL (Device, Sleep Assessment). Its devices cite 1 predicate, 0 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, neurology panel, where it files most

How often FDA has decided Neurim Pharmaceuticals, Ltd.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Neurim Pharmaceuticals, Ltd. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Neurim Pharmaceuticals, Ltd.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

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Which product codes does it file in?

  • LELDevice, Sleep Assessment1decision

Whose devices does it build on?

Its devices cite 1 predicate; 0 are its own earlier devices. The firms it cites most:

What has FDA decided for it lately?

  • K965079Somnitor 32K Sleep Activity MonitorNeurim Pharmaceuticals, Ltd. · 1997

The one decision as Neurim Pharmaceuticals, Ltd. →