Home / Companies / Astralite Corp.

Astralite Corp.

FDA Regulatory Profile

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