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Well Lead Medical Instruments

FDA Regulatory Profile

Well Lead Medical Instruments appears in FDA public data with 0 recalls, 4 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on October 8, 2008.

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

FDA data resources