# Physiq, Inc.

- Location (FDA's records): Naperville, IL
- FDA decisions: 3 (2018–2020): 3 510(k) clearances
- Product codes: DPS (3)
- 510(k) review time since 2016: median 193 days, against 221 for FDA's reviews in the same codes and years (2 of 3 faster)
- Predicates its devices cite: 4 (2 its own); citations of its devices by later devices: 3 (2 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Vitalconnect, Inc.: 1 (https://510kreport.com/company/vitalconnect)
- Monebo Technologies, Inc.: 1 (https://510kreport.com/company/monebo-technologies)

## Firms that cite its devices most
- Eko Devices, Inc.: 1 (https://510kreport.com/company/eko-devices)

## Its most-cited devices
- K180234: physiQ Heart Rhythm Module (2018), cited by 2
- K183322: physIQ Heart Rhythm and Respiratory Module (2019), cited by 1

## Recent decisions
- K193415: physIQ Heart Rhythm and Respiration Module (Jun 11, 2020)
- K183322: physIQ Heart Rhythm and Respiratory Module (Jul 10, 2019)
- K180234: physiQ Heart Rhythm Module (Aug 10, 2018)

Source page: https://510kreport.com/company/physiq