iSee (roflufocon D, roflufocon E) Daily Wear Orthokeratology Contact Lenses
Jan 2019
51d
C&E GP Specialist, Inc.
1
Total
1
Cleared
0
Denied
C&E GP Specialist, Inc. — FDA 510(k) Submissions
C&E GP Specialist, Inc. has submitted 1 FDA 510(k) premarket notifications since 2019, of which 1 received clearance as substantially equivalent to a predicate device.
The company's most frequent device categories include Lens, Contact (orthokeratology) . Use the specialty filter in the sidebar to narrow results.
1 devices