Automatic Wrist Bluetooth Blood Pressure Monitor
K-Number: K170545 · 2017-11-21
Device Summary
Frequently Asked Questions
What is the Automatic Wrist Bluetooth Blood Pressure Monitor?
Automatic Wrist Bluetooth Blood Pressure Monitor is a medical device that received FDA 510(k) clearance on 2017-11-21. The listed applicant is Truly Instrument , Ltd.. The 510(k) number is K170545.
When did Automatic Wrist Bluetooth Blood Pressure Monitor receive FDA 510(k) clearance?
Automatic Wrist Bluetooth Blood Pressure Monitor received FDA 510(k) clearance on 2017-11-21, under 510(k) number K170545.
Who is the listed applicant for Automatic Wrist Bluetooth Blood Pressure Monitor?
The FDA 510(k) record lists Truly Instrument , Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Automatic Wrist Bluetooth Blood Pressure Monitor?
The FDA product code for Automatic Wrist Bluetooth 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 Truly Instrument , 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.