QURASENSE, INC.
FDA Registration(s)#
Registration, FEI, Name table| Registration | FEI | Name | Status | Initial importer | Expiration year | Address |
|---|
| 3023949424 | 3023949424 | QURASENSE, INC. | 1 | N | 2026-01-01 | 3517 Edison Way Ste. D Menlo Park CA US 94025 |
Registered Device Listings#
Registration key, Listing key, Premarket submission table| Registration key | Listing key | Premarket submission | Device | Product code | Decision date |
|---|
| 308859 | 1904170388 | K231465 | Q-Pad Test System | LCP | 2023-12-06 |
Product Codes Associated With Registrations#
Product code, Registration listing records, Latest decision table| Product code | Registration listing records | Latest decision |
|---|
| LCP | 1 | 2023-12-06 |
GUDID#
Qurasense, Inc.
2026-05-08
Qurasense, Inc.
2026-05-08