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Physiq, Inc.

FDA Regulatory Profile

Physiq, Inc. has 0 FDA recalls, 1 inspection, 3 510(k) clearances and 0 compliance actions on record.

Latest inspection
Dec 18, 2019 · NAI
Latest 510(k)
Jun 11, 2020

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Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls0Oct 23, 2026Not statedCurrent
510(k) clearances3Oct 4, 2026Not statedCurrent
Inspections1Oct 25, 2026Not statedCurrent
Compliance actions0Oct 23, 2026Not statedCurrent

Recent FDA Inspections

DateSiteProductClassificationFEI
Dec 18, 2019Chicago, ILDevicesNo Action Indicated (NAI)3013414924

NAI means no objectionable conditions or practices were found during the inspection. VAI means objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action. OAI means regulatory and/or administrative actions are recommended.

Recent 510(k) Clearances

K-NumberDeviceDate
K193415physIQ Heart Rhythm and Respiration ModuleJun 11, 2020
K183322physIQ Heart Rhythm and Respiratory ModuleJul 10, 2019
K180234physiQ Heart Rhythm ModuleAug 10, 2018

FDA data resources