FDA 510(k) Applications for Medical Device Product Code "JTY"
(Culture Media, For Isolation Of Pathogenic Neisseria)

FDA 510(k) Number Applicant Device Name Decision Date
K210511 Biomed Diagnostics Incorporated InTray GC 10/20/2021
K993033 BIOMED DIAGNOSTICS, INC. INTRAY GC 12/16/1999
K954986 REMEL, L.P. GC BASE W/ 1% GCHI 02/16/1996


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