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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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