FDA applicant

Delsys, Inc.

Boston, MA3 decisions1995–19990 recalls

FDA records 3 decisions for Delsys, Inc. (Boston, MA) from 1995 to 1999: 3 510(k) clearances. All are in product code HCC (Device, Biofeedback). 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 Delsys, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Delsys, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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

See the 510(k) Report

Delsys, Inc.

Which product codes does it file in?

What has FDA decided for it lately?