Blood Pressure Monitor
K-Number: K200437 · 2020-06-25
Device Summary
Frequently Asked Questions
What is the Blood Pressure Monitor?
Blood Pressure Monitor is a medical device that received FDA 510(k) clearance on 2020-06-25. The listed applicant is Shenzhen Jamr Technology Co., Ltd.. The 510(k) number is K200437.
When did Blood Pressure Monitor receive FDA 510(k) clearance?
Blood Pressure Monitor received FDA 510(k) clearance on 2020-06-25, under 510(k) number K200437.
Who is the listed applicant for Blood Pressure Monitor?
The FDA 510(k) record lists Shenzhen Jamr Technology Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Blood Pressure Monitor?
The FDA product code for Blood Pressure Monitor is DXN.
Other records listing Shenzhen Jamr Technology Co., Ltd. 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.