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FDA 510(k)

Informed Vital Core Application (IVC App)

K-Number: K241633 · 2024-11-18

ApplicantMindset Medical, Inc.
Decision Date2024-11-18
Product CodeQME
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

Informed Vital Core Application (IVC App) is a medical device manufactured by Mindset Medical, Inc.. It received FDA 510(k) clearance on 2024-11-18 under approval number K241633. The device is classified under product code QME. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Informed Vital Core Application (IVC App)?

Informed Vital Core Application (IVC App) is a medical device that received FDA 510(k) clearance on 2024-11-18. It is manufactured by Mindset Medical, Inc.. The 510(k) number is K241633.

When was Informed Vital Core Application (IVC App) approved by the FDA?

Informed Vital Core Application (IVC App) received FDA 510(k) clearance on 2024-11-18, under approval number K241633.

What company makes Informed Vital Core Application (IVC App)?

Informed Vital Core Application (IVC App) is manufactured by Mindset Medical, Inc..

What is the FDA product code for Informed Vital Core Application (IVC App)?

The FDA product code for Informed Vital Core Application (IVC App) is QME.

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Other Devices by Mindset Medical, Inc.

K250078Informed Vital Core Application (IVC App) (v2.0.0.2.0.0)

Related Devices (Code: QME)

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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.

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