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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 the device name listed in this FDA 510(k) record. The listed applicant is Pursuant Health. It received FDA 510(k) clearance on 2024-01-04 under 510(k) 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. The listed applicant is Pursuant Health. The 510(k) number is K230996.

When did Pursuant Health Kiosk (G1.D5) receive FDA 510(k) clearance?

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

Who is the listed applicant for Pursuant Health Kiosk (G1.D5)?

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

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

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

Related Devices (Code: DXN)

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.

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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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