The primary objective of this clinical study is to collect clinical data to support FDA 510(k) submissions for the Topcon CT-800, CT-1, CT-1P and TRK-2P non-contact tonometers. The secondary objective is to evaluate any adverse events found during the clinical study.
Study Type
OBSERVATIONAL
Enrollment
65
Andover Eye Associates
Andover, Massachusetts, United States
Agreement of intraocular pressure measurements from predicate vs. investigational device
Time frame: Single timepoint - 1 day
Agreement of central corneal thickness measurements from predicate vs. investigational device
Time frame: Single time point - 1 day
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