FDA 510(k) Applications Submitted by HOSMAN INTERNATIONAL CO., LTD

FDA 510(k) Number Submission Date Device Name Applicant
K103046 10/14/2010 HOSMAN USB BLOOD PRESSURE MONITOR; WRIST TYPE AND UPPER ARM TYPE HOSMAN INTERNATIONAL CO., LTD


Search | Companies | Product Codes | Device Names | Contacts | Applications | Decisions | Contact