C&E GP Specialist, Inc. - FDA 510(k) Cleared Devices
Recent clearances: iSee (roflufocon D, roflufocon E) Daily Wear Orthokeratology Contact Lenses
1
Total
1
Cleared
0
Denied
FDA 510(k) Regulatory Record - C&E GP Specialist, Inc. Ophthalmic ✕
1 devices