GRF — Antiserum, Cf, Rubeola Class I
FDA Device Classification
Classification Details
- Product Code
- GRF
- Device Class
- Class I
- Regulation Number
- 866.3520
- Submission Type
- Review Panel
- MI
- Medical Specialty
- Microbiology
- Implant
- No
Recent 510(k) Clearances
| K-Number | Applicant | Device Name | Date |
|---|
| K922870 | osteo technology | THREE SPIKE CUP | April 8, 1993 |
| K852932 | microbix biosystems | MEASLES-COMPLEMENT FIX ANTIGEN & NEGATIVE CLT | November 12, 1985 |