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FDA 510(k)

BP-BT Kiosk

K-Number: K200287 · 2020-05-15

ApplicantLd Technology, LLC
Decision Date2020-05-15
Product CodeDXN
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

BP-BT Kiosk is the device name listed in this FDA 510(k) record. The listed applicant is Ld Technology, LLC. It received FDA 510(k) clearance on 2020-05-15 under 510(k) number K200287. 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 BP-BT Kiosk?

BP-BT Kiosk is a medical device that received FDA 510(k) clearance on 2020-05-15. The listed applicant is Ld Technology, LLC. The 510(k) number is K200287.

When did BP-BT Kiosk receive FDA 510(k) clearance?

BP-BT Kiosk received FDA 510(k) clearance on 2020-05-15, under 510(k) number K200287.

Who is the listed applicant for BP-BT Kiosk?

The FDA 510(k) record lists Ld Technology, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BP-BT Kiosk?

The FDA product code for BP-BT Kiosk is DXN.

Other records listing Ld Technology, LLC as applicant

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.

K200141Oxi-W SystemK173696TBL-ABI SystemK160956LD-Oxi system

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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