CHLAMYDIA-CEL IMMUNOFLUORENSCENCE (IF) TEST
May 1990
67d
Cel Labs Pty, Ltd.
1
Total
1
Cleared
0
Denied
Cel Labs Pty, Ltd. — FDA 510(k) Submissions
Cel Labs Pty, Ltd. has submitted 1 FDA 510(k) premarket notifications since 1990, of which 1 received clearance as substantially equivalent to a predicate device.
The company's most frequent device categories include Antiserum, Fluorescent, Chlamydia Trachomatis . Use the specialty filter in the sidebar to narrow results.
1 devices