Full Automatic (NIBP) Blood Pressure Monitor-HL158UB
K-Number: K190133 · 2019-06-13
Device Summary
Frequently Asked Questions
What is the Full Automatic (NIBP) Blood Pressure Monitor-HL158UB?
Full Automatic (NIBP) Blood Pressure Monitor-HL158UB is a medical device that received FDA 510(k) clearance on 2019-06-13. The listed applicant is Health & Life Co., Ltd.. The 510(k) number is K190133.
When did Full Automatic (NIBP) Blood Pressure Monitor-HL158UB receive FDA 510(k) clearance?
Full Automatic (NIBP) Blood Pressure Monitor-HL158UB received FDA 510(k) clearance on 2019-06-13, under 510(k) number K190133.
Who is the listed applicant for Full Automatic (NIBP) Blood Pressure Monitor-HL158UB?
The FDA 510(k) record lists Health & Life Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Full Automatic (NIBP) Blood Pressure Monitor-HL158UB?
The FDA product code for Full Automatic (NIBP) Blood Pressure Monitor-HL158UB 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 Health & Life 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.