| Device Type ID | 522 |
| Device Name | Diazo (colorimetric), Nitrite (urinary, Non-quant) |
| Regulation Description | Nitrite (nonquantitative) Test System. |
| Regulation Medical Specialty | Clinical Chemistry |
| Review Panel | Clinical Chemistry |
| Premarket Review | Office Of In Vitro Diagnostics And Radiological Health (OIR) |
| Submission Type | 510(K) Exempt |
| CFR Regulation Number | 862.1510 [🔎] |
| FDA Device Classification | Class 1 Medical Device |
| Product Code | JMT |
| GMP Exempt | No |
| Summary MR | Eligible |
| Implanted Device | No |
| Life Support Device | No |
| Third Party Review | Not Third Party Eligible |
|
| Device Type ID | 522 |
| Device | Diazo (colorimetric), Nitrite (urinary, Non-quant) |
| Product Code | JMT |
| FDA Device Classification | Class 1 Medical Device |
| Regulation Description | Nitrite (nonquantitative) Test System. |
| CFR Regulation Number | 862.1510 [🔎] |
| Device Problems | |
|---|---|
Incorrect, Inadequate Or Imprecise Result Or Readings | 1 |
| Total Device Problems | 1 |