Medical Device Manufacturer · US , Mchenry , IL

Dicon, Inc. - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 1981
4
Total
4
Cleared
0
Denied

FDA 510(k) Regulatory Record - Dicon, Inc. Ophthalmic ✕

4 devices
1-4 of 4
Cleared Sep 30, 1982
AUTO PERIOMETER 3000
K822580 · HPT
Ophthalmic · 36d
Cleared Jun 25, 1982
AUTOMATIC OBJECTIVE REFRACTOR 2000
K820877 · HKO
Ophthalmic · 87d
Cleared Aug 20, 1981
DICON AUTO PERIMETER 200
K811346 · HPT
Ophthalmic · 100d
Cleared Aug 20, 1981
DICON AUTO PERIMETER 2000
K811347 · HPT
Ophthalmic · 100d
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