FDA Registration
Active
🇺🇸 United States
LUMIQUICK DIAGNOSTICS, INC.
Reg #: 3005984081
·
FEI: 3005984081
·
Expires 2025
Products
6
Proprietary Names
0
Establishment Types
1
Classifications
6
Registration Details
- Registration Name
- LUMIQUICK DIAGNOSTICS, INC.
- Registration Number
- 3005984081
- FEI Number
- 3005984081
- Status
- Active
- Expiry Year
- 2025
- Initial Importer
- Yes
- Address
- 2946 SCOTT BLVD.
- City
- SANTA CLARA
- State
- CA
- ZIP
- 95054
- Country
- US
Regulatory Submissions
- 510(k) Number
- K003809
Owner / Operator
- Firm Name
- LUMIQUICK DIAGNOSTICS, INC.
- Operator Number
- 9093981
- Address
- 2946 SCOTT BLVD., --
- City
- Santa Clara
- State
- CA
- Postal Code
- 95054
- Country
- US
- Correspondent
- Chih C Wang
Products
| Device Name | Product Code | Device Class | Medical Specialty | Exempt | Created |
|---|---|---|---|---|---|
| Enzyme Immunoassay, Opiates | DJG | Class 2 | Clinical Toxicology | No | 2017-10-30 |
| Enzyme Immunoassay, Benzodiazepine | JXM | Class 2 | Clinical Toxicology | No | 2017-10-30 |
| Enzyme Immunoassay, Amphetamine | DKZ | Class 2 | Clinical Toxicology | No | 2017-10-30 |
| Thin Layer Chromatography, Methamphetamine | DJC | Class 2 | Clinical Toxicology | No | 2017-10-30 |
| Enzyme Immunoassay, Cocaine And Cocaine Metabolites | DIO | Class 2 | Clinical Toxicology | No | 2017-10-30 |
| Enzyme Immunoassay, Cannabinoids | LDJ | Class 2 | Clinical Toxicology | No | 2017-10-30 |
Establishment Types
Manufacture Medical Device