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Pluromed, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
4
Inspections
3
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K110491BACKSTOP CATHETERMarch 16, 2011
K103349BACKSTOP CATHETERJanuary 7, 2011
K090430BACKSTOP AND BACKSTOP INJECTORJune 2, 2009
K090270BACKSTOP CATHETER, MODEL 60-0000-3100May 15, 2009