JFR — Indirect Copper Assay, Ceruloplasmin Class II
FDA Device Classification
Classification Details
- Product Code
- JFR
- Device Class
- Class II
- Regulation Number
- 866.5210
- Submission Type
- Review Panel
- IM
- Medical Specialty
- Immunology
- Implant
- No
Recent 510(k) Clearances
| K-Number | Applicant | Device Name | Date |
|---|
| K051456 | sentinel ch | SENTINEL CERULOPLASMIN | October 21, 2005 |
| K882622 | technicon instruments | CERULOPLASMIN FOR THE TECHNICON DPA-1(TM) SYSTEM | July 8, 1988 |