FDA 510(k) Applications Submitted by MINDRAY NORTH AMERICA

FDA 510(k) Number Submission Date Device Name Applicant
K132037 07/01/2013 VITAL SIGNS MONITOR MINDRAY NORTH AMERICA
K132038 07/01/2013 ACCUTORR 7 VITAL SIGNS MONITOR MINDRAY NORTH AMERICA
K132075 07/03/2013 PASSPORT M SERIES PATIENT MONITORING (INCLUDING MODELS PASSPORT 17M AND PASSPORT 12M) MINDRAY NORTH AMERICA


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