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Percuvision, LLC

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
3
Inspections
2
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K110214DIRECTVISION CATHETER, UNCOATEDMay 27, 2011
K091600DIRECTVISION GUIDE SYSTEMAugust 25, 2009
K090262PERCUCATH URINARY CATHETERMay 28, 2009