FDA 510(k) Applications Submitted by VERATHON INCORPORATED

FDA 510(k) Number Submission Date Device Name Applicant
K090214 01/29/2009 VERATHON INC. BLADDERSCAN BVM 9500 ULTRASOUND VERATHON INCORPORATED
K153101 10/26/2015 BladderScan Prime System VERATHON INCORPORATED
K082456 08/26/2008 VERATHON INC. BLADDERSCAN ULTRASOUND SYSTEM, MODEL BVI 9600 VERATHON INCORPORATED
K071217 05/02/2007 BLADDERSCAN BVI 9400 ULTRASOUND VERATHON INCORPORATED
K172356 08/03/2017 BladderScan Prime PLUS System Verathon Incorporated


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