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Bard Medical Div.

FDA Regulatory Profile

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K984136BARDEX LUBRI-SIL I.C. FOLEY CATHETERFebruary 16, 1999
K984084BARDEX LUBRI-SIL FOLEY CATHETERFebruary 1, 1999
K970110BARD FLEXIBLE ENDOSCOPY INJECTION SYSTEM (651019)February 19, 1997