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The Lebanon Corp.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
3
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K841652OCULAR PRESSURE APPLICATORJune 1, 1984
K821689LEBANON MICROSCOPEJuly 9, 1982
K820526RELIEF VALVE-HONAN INTRAOC. PRESSUREMarch 25, 1982