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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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