FDA applicant
Physiq, Inc.
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
How often FDA has decided Physiq, Inc.’s devices, and how often a recall has named them.
FDA decisions per year
1in 2020
2026 so far, outlined.
Recalls per year
No recall linked to its devices since 2018.
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.
See the 510(k) Report