9
Total
9
Cleared
0
Denied

Ocu-Ease Optical Products, Inc. has 9 FDA 510(k) cleared medical devices. Based in Pinole, US.

Historical record: 9 cleared submissions from 1994 to 2002. Primary specialty: Ophthalmic.

Browse the FDA 510(k) cleared devices submitted by Ocu-Ease Optical Products, Inc. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Ocu-Ease Optical Products, Inc.

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