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 a medical device manufactured by Ld Technology, LLC. It received FDA 510(k) clearance on 2020-05-15 under approval 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. It is manufactured by Ld Technology, LLC. The 510(k) number is K200287.
When was BP-BT Kiosk approved by the FDA?
BP-BT Kiosk received FDA 510(k) clearance on 2020-05-15, under approval number K200287.
What company makes BP-BT Kiosk?
BP-BT Kiosk is manufactured by Ld Technology, LLC.
What is the FDA product code for BP-BT Kiosk?
The FDA product code for BP-BT Kiosk is DXN.
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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.