| Device Type ID | 6023 |
| Device Name | Lead, Delta Amino Levulinic Acid |
| Regulation Description | Lead Test System. |
| Regulation Medical Specialty | Toxicology |
| Review Panel | Toxicology |
| Premarket Review | Office Of In Vitro Diagnostics And Radiological Health (OIR) |
| Submission Type | 510(k) |
| CFR Regulation Number | 862.3550 [🔎] |
| FDA Device Classification | Class 2 Medical Device |
| Product Code | DIJ |
| GMP Exempt | No |
| Summary MR | Eligible |
| Implanted Device | No |
| Life Support Device | No |
| Third Party Review | Eligible For Accredited Persons Expansion Pilot Program |
| Device Type ID | 6023 |
| Device | Lead, Delta Amino Levulinic Acid |
| Product Code | DIJ |
| FDA Device Classification | Class 2 Medical Device |
| Regulation Description | Lead Test System. |
| CFR Regulation Number | 862.3550 [🔎] |