Aneroid Sphygmomanometer— 510(k) K230859

Substantially Equivalent

Wenzhou Kangshun Medical Devices Co.,Ltd

FDA 510(k) clearance K230859 for Aneroid Sphygmomanometer, Substantially Equivalent on 2023-06-28. Applicant: Wenzhou Kangshun Medical Devices Co.,Ltd. Device class: 2.

Clearance details

Applicant
Wenzhou Kangshun Medical Devices Co.,Ltd
Product code
Code DXQ
Device class
Class 2
Regulation
21 CFR 870.1120
Advisory panel
Cardiovascular
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Wenzhou City, CN
Download summary PDFView on FDA.gov ↗

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