| Device Type ID | 3393 |
| Device Name | Device, Oxidase Test For Gonorrhea |
| Regulation Description | Oxidase Screening Test For Gonorrhea. |
| Regulation Medical Specialty | Microbiology |
| Review Panel | Microbiology |
| Premarket Review | Office Of In Vitro Diagnostics And Radiological Health (OIR) |
| Submission Type | PMA |
| CFR Regulation Number | 866.2420 [🔎] |
| FDA Device Classification | Class 3 Medical Device |
| Product Code | LGA |
| GMP Exempt | No |
| Summary MR | Ineligible |
| Implanted Device | No |
| Life Support Device | No |
| Third Party Review | Not Third Party Eligible |
| Device Type ID | 3393 |
| Device | Device, Oxidase Test For Gonorrhea |
| Product Code | LGA |
| FDA Device Classification | Class 3 Medical Device |
| Regulation Description | Oxidase Screening Test For Gonorrhea. |
| CFR Regulation Number | 866.2420 [🔎] |