FDA applicant

Philips Park

Essex, CT11 decisions1984–19860 recalls

FDA records 11 decisions for Philips Park (Essex, CT) from 1984 to 1986: 11 510(k) clearances. Most are in product codes DXN (System, Measurement, Blood-Pressure…) and FLL (Continuous Measurement Thermometer). 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 Philips Park’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Philips Park since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Philips Park’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

Philips Park

Which product codes does it file in?

What has FDA decided for it lately?