Aurora
Sodium Systems, LLC
SODIUM SYSTEMS, LLC
FDA Registration(s)
| Registration | FEI | Name | Status | Initial importer | Expiration year | Address |
|---|---|---|---|---|---|---|
| 3014529181 | 3014529181 | SODIUM SYSTEMS, LLC | 1 | N | 2020-04-25 | 1050 Highland Drive Suite E Ann Arbor MI US 48108 |
Registered Device Listings
| Registration key | Listing key | Premarket submission | Device | Product code | Decision date |
|---|---|---|---|---|---|
| 220912 | 1609890021 | K181636 | Aurora | MUH | 2018-07-20 |
Product Codes Associated With Registrations
| Product code | Registration listing records | Latest decision |
|---|---|---|
| MUH | 1 | 2018-07-20 |
PMN
GUDID
Aurora - Aurora Size 1
2018-10-25
Aurora - Aurora Size 2
2018-10-25