Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

Care Team Portal

K-Number: K222398 · 2023-02-06

Decision Date2023-02-06
Product CodeDRG
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

Care Team Portal is the device name listed in this FDA 510(k) record. The listed applicant is Vivify Health, Inc.. It received FDA 510(k) clearance on 2023-02-06 under 510(k) number K222398. The device is classified under product code DRG. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Care Team Portal?

Care Team Portal is a medical device that received FDA 510(k) clearance on 2023-02-06. The listed applicant is Vivify Health, Inc.. The 510(k) number is K222398.

When did Care Team Portal receive FDA 510(k) clearance?

Care Team Portal received FDA 510(k) clearance on 2023-02-06, under 510(k) number K222398.

Who is the listed applicant for Care Team Portal?

The FDA 510(k) record lists Vivify Health, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Care Team Portal?

The FDA product code for Care Team Portal is DRG.

Related Devices (Code: DRG)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.