RM Electrode (RMH 23-01)
Retmap, Inc.
RETMAP, INC.
FDA Registration(s)#
| Registration | FEI | Name | Status | Initial importer | Expiration year | Address |
|---|---|---|---|---|---|---|
| 3033274216 | 3033274216 | RETMAP, INC. | 1 | N | 2026-01-01 | 832 W Superior St # 202e Chicago IL US 60642 |
Registered Device Listings#
| Registration key | Listing key | Premarket submission | Device | Product code | Decision date |
|---|---|---|---|---|---|
| 332965 | 1621893008 | K232273 | RM Electrode (RMH 23-01) | HLZ | 2023-12-07 |
Product Codes Associated With Registrations#
| Product code | Registration listing records | Latest decision |
|---|---|---|
| HLZ | 1 | 2023-12-07 |