Gkc Manufacturing Pty, Ltd.
FDA 510(k) & PMA Approved Devices — 2 products
Total Devices2
Categories1
Latest FDA decision2022-03-11
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K211887 | Personal Kinetigraph (PKG) System Gen 2 Plus | GYD | 2022-03-11 | View |
| 510(k) | K161717 | Personal Kinetigraph (PKG) System | GYD | 2016-09-20 | View |
No matching devices.