FDA 510(k) Applications Submitted by SUREFIRE MEDICAL, INC

FDA 510(k) Number Submission Date Device Name Applicant
K110459 02/17/2011 SUREFIRE INFUSION CATHETER SYSTEM SUREFIRE MEDICAL, INC
K160662 03/09/2016 Surefire Infusion System SUREFIRE MEDICAL, INC
K143588 12/18/2014 Surefire Infusion System 021 SUREFIRE MEDICAL, INC
K122506 08/17/2012 SUREFIRE HIGH FLOW ANGIOGRAPHIC CATHETER, ACCESS SUREFIRE MEDICAL, INC
K113737 12/20/2011 SUREFIRE GUIDE SHEATH SUREFIRE MEDICAL, INC


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