FDA 510(k) Applications for Medical Device Product Code "JTY"
|
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 |