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FDA 510(k)

HEALTH CHECK KIOSK

K-Number: K063008 · 2007-06-07

ApplicantXperex Corporation
Decision Date2007-06-07
Product CodeDXN
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

HEALTH CHECK KIOSK is the device name listed in this FDA 510(k) record. The listed applicant is Xperex Corporation. It received FDA 510(k) clearance on 2007-06-07 under 510(k) number K063008. 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 HEALTH CHECK KIOSK?

HEALTH CHECK KIOSK is a medical device that received FDA 510(k) clearance on 2007-06-07. The listed applicant is Xperex Corporation. The 510(k) number is K063008.

When did HEALTH CHECK KIOSK receive FDA 510(k) clearance?

HEALTH CHECK KIOSK received FDA 510(k) clearance on 2007-06-07, under 510(k) number K063008.

Who is the listed applicant for HEALTH CHECK KIOSK?

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

What is the FDA product code for HEALTH CHECK KIOSK?

The FDA product code for HEALTH CHECK KIOSK is DXN.

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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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