GRE — Antiserum, Fluorescent, Rubeola Class I
FDA Device Classification
Classification Details
- Product Code
- GRE
- 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 |
|---|
| K884004 | gull laboratories | RUBEOLA TEST | December 5, 1988 |
| K853067 | idt, a division of whittaker m.a. bioproducts | FIAX TEST KIT FOR MEASLES-G ANTIBODIES FLYORESCENT | October 22, 1985 |
| K821249 | electro-nucleonics laboratories | ENI ANTIBODY TO MEASLES(RUBEOLA) VIRUS | July 30, 1982 |
| K770687 | microbiological assoc | MEASLESVIRUS FLOURE. CONJUGATED ANTISERU | June 14, 1977 |