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Astralite Corp.

FDA Regulatory Profile

Astralite Corp. appears in FDA public data with 0 recalls, 2 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on January 28, 2003.

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K023004LFRE INDIRECT LARYNGOSCOPEJanuary 28, 2003
K893813FLOOR STANDING, OPERATING AND EXAMINING LIGHTJuly 14, 1989

FDA data resources