Home / Companies / Isolux America

Isolux America

FDA Regulatory Profile

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K022384XENON FIBEROPTIC LIGHT SOURCE, MODEL 1300 XSBPOctober 18, 2002
K991572ISOLUX SURGICAL HEADLIGHTJuly 8, 1999
K991208ENDOSCOPIC FIBEROPTIC CABLEJune 23, 1999