VMRD, Inc.
FDA Registration(s)#
| Registration | FEI | Name | Status | Initial importer | Expiration year | Address |
|---|---|---|---|---|---|---|
| 3004036192 | 3004036192 | VMRD, Inc. | 1 | N | 2026-01-01 | 1312 E Valencia Dr FULLERTON CA US 92831 |
Registered Device Listings#
| Registration key | Listing key | Premarket submission | Device | Product code | Decision date |
|---|---|---|---|---|---|
| 335611 | 1832064133 | K925690 | MERIDIAN EBNA TEST KIT | LLM | 1993-10-12 |
| 335611 | 1085932444 | ||||
| 335611 | 1154809606 | ||||
| 335611 | 1226314800 | ||||
| 335611 | 1310106132 | ||||
| 335611 | 1434208761 | ||||
| 335611 | 1586712477 | ||||
| 335611 | 1740953002 | ||||
| 335611 | 1761089912 | ||||
| 335611 | 2052814998 |
Product Codes Associated With Registrations#
| Product code | Registration listing records | Latest decision |
|---|---|---|
| LLM | 1 | 1993-10-12 |