KJR — Erythrosin B Class I
FDA Device Classification
Classification Details
- Product Code
- KJR
- Device Class
- Class I
- Regulation Number
- 864.1850
- Submission Type
- Review Panel
- PA
- Medical Specialty
- Hematology
- Implant
- No
Recent 510(k) Clearances
| K-Number | Applicant | Device Name | Date |
|---|
| K842834 | bartels immunodiagnostic supplies | HEP-2 CELLS | August 28, 1984 |
| K842833 | bartels immunodiagnostic supplies | PMK PRIMARY MONKEY KIDNEY-CELLS | August 28, 1984 |
| K792546 | alta diagnostics | FETAL CHECK | December 18, 1979 |