GRB — Antiserum, Cf, Mumps Virus Class I
FDA Device Classification
Classification Details
- Product Code
- GRB
- Device Class
- Class I
- Regulation Number
- 866.3380
- Submission Type
- Review Panel
- MI
- Medical Specialty
- Microbiology
- Implant
- No
Recent 510(k) Clearances
| K-Number | Applicant | Device Name | Date |
|---|
| K872733 | whittaker bioproducts | FIAX TEST KIT FOR MUMPS-G ANTIBODIES | October 6, 1987 |
| K872699 | sita | MUMPS CF ANTIGEN AND CONTROL ANTIGEN | September 18, 1987 |