Elecrtronic Blood Pressure Monitor (BP-201, BP-202, BP-203, BP-204, BP-205, BP-206)
K-Number: K241613 · 2024-10-16
Device Summary
Frequently Asked Questions
What is the Elecrtronic Blood Pressure Monitor (BP-201, BP-202, BP-203, BP-204, BP-205, BP-206)?
Elecrtronic Blood Pressure Monitor (BP-201, BP-202, BP-203, BP-204, BP-205, BP-206) is a medical device that received FDA 510(k) clearance on 2024-10-16. The listed applicant is Shenzhen Hbcare Technology Co.,Ltd. The 510(k) number is K241613.
When did Elecrtronic Blood Pressure Monitor (BP-201, BP-202, BP-203, BP-204, BP-205, BP-206) receive FDA 510(k) clearance?
Elecrtronic Blood Pressure Monitor (BP-201, BP-202, BP-203, BP-204, BP-205, BP-206) received FDA 510(k) clearance on 2024-10-16, under 510(k) number K241613.
Who is the listed applicant for Elecrtronic Blood Pressure Monitor (BP-201, BP-202, BP-203, BP-204, BP-205, BP-206)?
The FDA 510(k) record lists Shenzhen Hbcare Technology Co.,Ltd as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Elecrtronic Blood Pressure Monitor (BP-201, BP-202, BP-203, BP-204, BP-205, BP-206)?
The FDA product code for Elecrtronic Blood Pressure Monitor (BP-201, BP-202, BP-203, BP-204, BP-205, BP-206) is DXN.
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.