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Aculux, Inc.

FDA Regulatory Profile

Aculux, Inc. appears in FDA public data with 0 recalls, 2 510(k) clearances, 4 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on February 1, 2002.

Summary

Total Recalls
0
510(k) Clearances
2
Inspections
4
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K013511XENALIGHT MODELS # AX9125 (100-120V~); # AX9225 (220-240V~)February 1, 2002
K001223ACULUX, MODEL AX3001, AX3002June 23, 2000

FDA data resources