The Linden Group Corp
FDA 510(k) & PMA Approved Devices — 2 products
Total Devices2
Categories1
Latest FDA decision2020-03-16
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K191705 | OptikView GUP2103CMI | PGY | 2020-03-16 | View |
| 510(k) | K160328 | DIVA ZSP2105CMI with QUBYX PerfectLum bundle | PGY | 2016-02-25 | View |
No matching devices.