Gkc Manufacturing Pty, Ltd. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Gkc Manufacturing Pty, Ltd. - FDA 510(k) Cleared Devices
Recent clearances: Personal Kinetigraph (PKG) System Gen 2 Plus
3
Total
3
Cleared
0
Denied
Gkc Manufacturing Pty, Ltd. has 3 FDA 510(k) cleared medical devices. Based in Rockville, US.
Last cleared in 2022. Active since 2014. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Gkc Manufacturing Pty, Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by DuVal & Associates, P.A. as regulatory consultant.
FDA 510(k) Regulatory Record - Gkc Manufacturing Pty, Ltd.
3 devices