Verathon Incorporated - FDA 510(k) Cleared Devices
Recent clearances: BladderScan Prime PLUS System, BladderScan Prime System
5
Total
5
Cleared
0
Denied
FDA 510(k) Regulatory Record - Verathon Incorporated Radiology ✕
5 devices
Cleared
Sep 15, 2017
BladderScan Prime PLUS System
Radiology
43d
Cleared
Nov 19, 2015
BladderScan Prime System
Radiology
24d
Cleared
Mar 13, 2009
VERATHON INC. BLADDERSCAN BVM 9500 ULTRASOUND
Radiology
43d
Cleared
Dec 01, 2008
VERATHON INC. BLADDERSCAN ULTRASOUND SYSTEM, MODEL BVI 9600
Radiology
97d
Cleared
May 17, 2007
BLADDERSCAN BVI 9400 ULTRASOUND
Radiology
15d