Applied Technology Ventures, LLC
FDA 510(k) & PMA Approved Devices — 2 products
Advertisement
Total Devices2
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K980836 | GENIE CUP INTEGRATED SCREENING DEVICE | LDJ | 1998-06-29 | View |
| 510(k) | K973726 | FINGERPRINT DRUG SCREENING DEVICE | DKZ | 1997-11-06 | View |
No matching devices.
Advertisement