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510k Database
Manufacturers
US
The Lebanon Corp.
Medical Device Manufacturer
·
US , Mchenry , IL
The Lebanon Corp. - FDA 510(k) Cleared Devices
3 submissions
·
3 cleared
·
Since 1982
3
Total
3
Cleared
0
Denied
FDA 510(k) Regulatory Record - The Lebanon Corp.
Ophthalmic
✕
2
devices
1-2 of 2
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Cleared
Jun 01, 1984
OCULAR PRESSURE APPLICATOR
K841652
Ophthalmic
·
42d
Cleared
Mar 25, 1982
RELIEF VALVE-HONAN INTRAOC. PRESSURE
K820526
·
LCC
Ophthalmic
·
27d
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3
Ophthalmic
2
General & Plastic Surgery
1