510(k) K260066

Device
PanopticAI Vital Signs (1.6.1-22)
Applicant
PanopticAI Technologies Limited
510(k) number
K260066
Product code
QME
Decision
Substantially Equivalent (SESE)
Decision date
2026-05-21
Date received
2026-01-09
Regulation
870.2785
Classification name
Software For Optical Camera-Based Measurement Of Pulse Rate, Heart Rate, Breathing Rate, And/Or Respiratory Rate
Medical specialty
Cardiovascular
Review panel
Cardiovascular
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
N

Applicant Contact#

Contact
Nick Chin
Address
Rm. A, Ground Floor, 3 Tin Hau Temple Rd. North Pt. Hong Kong HK

FDA Registration Numbers#

Source Documents#

510(k) summary PDF

Other 510(k) Records For Product Code QME#

510(k), Device, Applicant table
510(k)DeviceApplicantDecision date
K251200Vital SignsOxehealth Limited2026-02-02
K243687Vital SignsOxehealth Limited2025-08-27
K250078Informed Vital Core Application (IVC App) (v2.0.0.2.0.0)Mindset Medical, Inc.2025-05-30
K240890PanopticAI Vital SignsPanopticAI technologies Limited2024-12-23
K241633Informed Vital Core Application (IVC App)Mindset Medical, Inc.2024-11-18
K232804FibriCheckQompium NV2024-06-07
K223622FaceHeart Vitals Software Development Kit (FH vitals SDK)Faceheart Corp.2023-09-01
K220899Oxehealth Vital SignsOxehealth Limited2022-04-29
K211906Vital SignsOxehealth Limited2021-07-20
DEN200019Oxehealth Vital SignsOxehealth Limited2021-03-26