Aneroid Sphygmomanometer; Single Patient Use Aneroid Sphygmomanometer
K-Number: K222652 · 2022-11-28
Device Summary
Frequently Asked Questions
What is the Aneroid Sphygmomanometer; Single Patient Use Aneroid Sphygmomanometer?
Aneroid Sphygmomanometer; Single Patient Use Aneroid Sphygmomanometer is a medical device that received FDA 510(k) clearance on 2022-11-28. The listed applicant is Cardicare Company, Ltd.. The 510(k) number is K222652.
When did Aneroid Sphygmomanometer; Single Patient Use Aneroid Sphygmomanometer receive FDA 510(k) clearance?
Aneroid Sphygmomanometer; Single Patient Use Aneroid Sphygmomanometer received FDA 510(k) clearance on 2022-11-28, under 510(k) number K222652.
Who is the listed applicant for Aneroid Sphygmomanometer; Single Patient Use Aneroid Sphygmomanometer?
The FDA 510(k) record lists Cardicare Company, Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Aneroid Sphygmomanometer; Single Patient Use Aneroid Sphygmomanometer?
The FDA product code for Aneroid Sphygmomanometer; Single Patient Use Aneroid Sphygmomanometer is DXQ.
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.