510(k) Report

FDA applicant

Physiq, Inc.

Naperville, IL3 decisions2018–20200 recalls

FDA records 3 decisions for Physiq, Inc. (Naperville, IL) from 2018 to 2020: 3 510(k) clearances. All are in product code DPS (Electrocardiograph). Since 2016 its 510(k)s took a median of 193 days from receipt to decision, against 221 for FDA’s reviews in the same codes and years. Its devices cite 4 predicates, 2 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 Physiq, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2020

2018: 12019: 12020: 1
2018high 1 (2018) · low 0 (2021)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2018.

FIG. 1 — Physiq, Inc. by year, 2018–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Physiq, Inc.’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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