| Device Type ID | 4766 |
| Device Name | Giemsa Stain |
| Regulation Description | Dye And Chemical Solution Stains. |
| Regulation Medical Specialty | Hematology |
| Review Panel | Pathology |
| Premarket Review | Office Of In Vitro Diagnostics And Radiological Health (OIR) |
| Submission Type | 510(K) Exempt |
| CFR Regulation Number | 864.1850 [🔎] |
| FDA Device Classification | Class 1 Medical Device |
| Product Code | HYF |
| GMP Exempt | Yes |
| Summary MR | Eligible |
| Implanted Device | No |
| Life Support Device | No |
| Third Party Review | Not Third Party Eligible |
| Device Type ID | 4766 |
| Device | Giemsa Stain |
| Product Code | HYF |
| FDA Device Classification | Class 1 Medical Device |
| Regulation Description | Dye And Chemical Solution Stains. |
| CFR Regulation Number | 864.1850 [🔎] |
| Recalls | |||
|---|---|---|---|
| Manufacturer | Recall Class | Date Posted | |
| 1 | Richard-Allan Scientific Company | II | Apr-17-2017 |