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FDA 510(k)

Pursuant Health Kiosk (G1.D5)

K-Number: K230996 · 2024-01-04

ApplicantPursuant Health
Decision Date2024-01-04
Product CodeDXN
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

Pursuant Health Kiosk (G1.D5) is a medical device manufactured by Pursuant Health. It received FDA 510(k) clearance on 2024-01-04 under approval number K230996. The device is classified under product code DXN. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Pursuant Health Kiosk (G1.D5)?

Pursuant Health Kiosk (G1.D5) is a medical device that received FDA 510(k) clearance on 2024-01-04. It is manufactured by Pursuant Health. The 510(k) number is K230996.

When was Pursuant Health Kiosk (G1.D5) approved by the FDA?

Pursuant Health Kiosk (G1.D5) received FDA 510(k) clearance on 2024-01-04, under approval number K230996.

What company makes Pursuant Health Kiosk (G1.D5)?

Pursuant Health Kiosk (G1.D5) is manufactured by Pursuant Health.

What is the FDA product code for Pursuant Health Kiosk (G1.D5)?

The FDA product code for Pursuant Health Kiosk (G1.D5) is DXN.

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Official Source

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

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