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FDA 510(k) Applications Submitted by Surefire Medical, Inc.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K140034
01/07/2014
SUREFIRE GUIDING CATHETER
SUREFIRE MEDICAL, INC.
K180677
03/15/2018
Surefire Spark Infusion System
Surefire Medical, Inc.
K171355
05/09/2017
Surefire Precision Infusion System
Surefire Medical, Inc.
K162359
08/23/2016
Surefire Guiding Catheter
Surefire Medical, Inc.
K121677
06/07/2012
SUREFIRE HI-FLOW MICROCATHETER
SUREFIRE MEDICAL, INC.
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