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Percutaneous Systems, Incorporated

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
5
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K090485COAXIAL ACCORDION ERCP DEVICE, MODELS C0AC19001, COAC20005, COAC22003July 22, 2009
K061766EXPRESSWAY INTERMITTENT CATHETERMarch 9, 2007
K052298CYSTOGLIDE INTRODUCER SHEATHDecember 12, 2006
K052048ACCORDIONSeptember 13, 2005
K042531UPDATED SLIP UROLOGY INTRODUCER SHEATHFebruary 1, 2005