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Orbtek, Inc.

FDA Regulatory Profile

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K964891ORBSHOT KERATOMETERMarch 26, 1997
K940647ORBSCAN(TM) KERATOMETERJuly 6, 1994