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FDA 510(k)

Microlife Upper Arm Automatic Digital Blood Pressure Monitor, Model BP3KVl-5K

K-Number: K230075 · 2023-06-28

Decision Date2023-06-28
Product CodeDXN
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

Microlife Upper Arm Automatic Digital Blood Pressure Monitor, Model BP3KVl-5K is the device name listed in this FDA 510(k) record. The listed applicant is Microlife Intellectual Property GmbH. It received FDA 510(k) clearance on 2023-06-28 under 510(k) number K230075. 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 Microlife Upper Arm Automatic Digital Blood Pressure Monitor, Model BP3KVl-5K?

Microlife Upper Arm Automatic Digital Blood Pressure Monitor, Model BP3KVl-5K is a medical device that received FDA 510(k) clearance on 2023-06-28. The listed applicant is Microlife Intellectual Property GmbH. The 510(k) number is K230075.

When did Microlife Upper Arm Automatic Digital Blood Pressure Monitor, Model BP3KVl-5K receive FDA 510(k) clearance?

Microlife Upper Arm Automatic Digital Blood Pressure Monitor, Model BP3KVl-5K received FDA 510(k) clearance on 2023-06-28, under 510(k) number K230075.

Who is the listed applicant for Microlife Upper Arm Automatic Digital Blood Pressure Monitor, Model BP3KVl-5K?

The FDA 510(k) record lists Microlife Intellectual Property GmbH as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Microlife Upper Arm Automatic Digital Blood Pressure Monitor, Model BP3KVl-5K?

The FDA product code for Microlife Upper Arm Automatic Digital Blood Pressure Monitor, Model BP3KVl-5K is DXN.

Related Clinical Trials

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.

Other records listing Microlife Intellectual Property GmbH 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.

View all 18 devices →

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.

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.