Reusable Blood Pressure Cuff
K-Number: K233276 · 2023-12-21
Device Summary
Frequently Asked Questions
What is the Reusable Blood Pressure Cuff?
Reusable Blood Pressure Cuff is a medical device that received FDA 510(k) clearance on 2023-12-21. The listed applicant is Suzhou Minhua Medical Apparatus Supplies Co., Ltd.. The 510(k) number is K233276.
When did Reusable Blood Pressure Cuff receive FDA 510(k) clearance?
Reusable Blood Pressure Cuff received FDA 510(k) clearance on 2023-12-21, under 510(k) number K233276.
Who is the listed applicant for Reusable Blood Pressure Cuff?
The FDA 510(k) record lists Suzhou Minhua Medical Apparatus Supplies Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Reusable Blood Pressure Cuff?
The FDA product code for Reusable Blood Pressure Cuff is DXQ.
Other records listing Suzhou Minhua Medical Apparatus Supplies 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: DXQ)
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.