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Isolux America

FDA Regulatory Profile

Isolux America appears in FDA public data with 0 recalls, 3 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on October 18, 2002.

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

FDA data resources