Microlife Upper Arm Automatic Digital Blood Pressure Monitor, Model BP3KVl-5K
K-Number: K230075 · 2023-06-28
Device Summary
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.
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
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.