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 |