510(k) K222398

Device
Care Team Portal
Applicant
Vivify Health, Inc.
510(k) number
K222398
Product code
DRG
Decision
Substantially Equivalent (SESE)
Decision date
2023-02-06
Date received
2022-08-08
Regulation
870.2910
Classification name
Transmitters And Receivers, Physiological Signal, Radiofrequency
Medical specialty
Cardiovascular
Review panel
Cardiovascular
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
No

Related Records

Applicant Contact

Contact
Tracey Fox
Address
7201 Bishop Rd. Suite #E200 Plano TX US 75024 75024

FDA Registration Numbers

Source Documents

510(k) summary PDF

Related GUDID Devices

Primary DIBrandCompanyPublished
00850032055246Vivify Health Care Team Portal 001Vivify Health, Inc.2024-02-19
00850032055185Vivifyhealth SK005Vivify Health, Inc.2024-02-19

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