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Well Lead Medical Instruments

FDA Regulatory Profile

Summary

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

Known Names

well lead medical instruments, well lead medical instruments co

Recent 510(k) Clearances

K-NumberDeviceDate
K082815WELL LEAD SILICONE AND LATEX FOLEY CATHETERSOctober 8, 2008
K073383WELL LEAD REINFORCED ENDOTRACHEAL TUBEJuly 10, 2008
K042683WELL LEAD ENDOTRACHEAL TUBEFebruary 18, 2005
K042684WELL LEAD TRACHEOSTOMY TUBEFebruary 17, 2005