Aneroid Sphygmomanometer with Stethoscope; Aneroid Sphygmomanometer
K-Number: K240165 · 2024-03-20
Device Summary
Frequently Asked Questions
What is the Aneroid Sphygmomanometer with Stethoscope; Aneroid Sphygmomanometer?
Aneroid Sphygmomanometer with Stethoscope; Aneroid Sphygmomanometer is a medical device that received FDA 510(k) clearance on 2024-03-20. The listed applicant is Wenzhou Longwan Medical Device Factory. The 510(k) number is K240165.
When did Aneroid Sphygmomanometer with Stethoscope; Aneroid Sphygmomanometer receive FDA 510(k) clearance?
Aneroid Sphygmomanometer with Stethoscope; Aneroid Sphygmomanometer received FDA 510(k) clearance on 2024-03-20, under 510(k) number K240165.
Who is the listed applicant for Aneroid Sphygmomanometer with Stethoscope; Aneroid Sphygmomanometer?
The FDA 510(k) record lists Wenzhou Longwan Medical Device Factory as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Aneroid Sphygmomanometer with Stethoscope; Aneroid Sphygmomanometer?
The FDA product code for Aneroid Sphygmomanometer with Stethoscope; 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.