CLEARSPEC SINGLE USE VAGINAL SPECULUM
Aug 2013
210d
Clearspec, LLC
1
Total
1
Cleared
0
Denied
Clearspec, LLC — FDA 510(k) Submissions
Clearspec, LLC has submitted 1 FDA 510(k) premarket notifications since 2013, of which 1 received clearance as substantially equivalent to a predicate device.
The company's most frequent device categories include Speculum, Vaginal, Nonmetal . Use the specialty filter in the sidebar to narrow results.
1 devices