| Device Type ID | 3406 |
| Device Name | Antisera, Conjugated Fluorescent, Cytomegalovirus |
| Regulation Description | Cytomegalovirus Serological Reagents. |
| Regulation Medical Specialty | Microbiology |
| Review Panel | Microbiology |
| Premarket Review | Office Of In Vitro Diagnostics And Radiological Health (OIR) |
| Submission Type | 510(k) |
| CFR Regulation Number | 866.3175 [🔎] |
| FDA Device Classification | Class 2 Medical Device |
| Product Code | LIN |
| 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 | 3406 |
| Device | Antisera, Conjugated Fluorescent, Cytomegalovirus |
| Product Code | LIN |
| FDA Device Classification | Class 2 Medical Device |
| Regulation Description | Cytomegalovirus Serological Reagents. |
| CFR Regulation Number | 866.3175 [🔎] |
| Device Problems | |
|---|---|
High Test Results | 3 |
Cell | 1 |
Low Test Results | 1 |
| Total Device Problems | 5 |