Upper Arm Type Blood Pressure Monitor
K-Number: K220886 · 2022-07-27
Device Summary
Frequently Asked Questions
What is the Upper Arm Type Blood Pressure Monitor?
Upper Arm Type Blood Pressure Monitor is a medical device that received FDA 510(k) clearance on 2022-07-27. The listed applicant is Shenzhen Jamr Technology Co., Ltd.. The 510(k) number is K220886.
When did Upper Arm Type Blood Pressure Monitor receive FDA 510(k) clearance?
Upper Arm Type Blood Pressure Monitor received FDA 510(k) clearance on 2022-07-27, under 510(k) number K220886.
Who is the listed applicant for Upper Arm Type 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 Upper Arm Type Blood Pressure Monitor?
The FDA product code for Upper Arm Type Blood Pressure Monitor 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 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.