GRE
4 FDA 510(k) clearances · Product code
FDA profile
- Official device name
- Antiserum, Fluorescent, Rubeola
- Device class
- Class I (low risk)
- Regulation
- 21 CFR 866.3520
- Medical specialty
- Microbiology
Export predicate table (CSV) Shareable report ◉ Watch exports: 3 free/month · reports & watching: free
| Record | Firm | Date |
|---|---|---|
| RUBEOLA TEST (K884004) | Gull Laboratories, Inc. | 1988-12-05 |
| FIAX TEST KIT FOR MEASLES-G ANTIBODIES FLYORESCENT (K853067) | Idt, A Division of Whittaker M.A. Bioproducts | 1985-10-22 |
| ENI ANTIBODY TO MEASLES(RUBEOLA) VIRUS (K821249) | Electro-Nucleonics Laboratories, Inc. | 1982-07-30 |
| MEASLESVIRUS FLOURE. CONJUGATED ANTISERU (K770687) | Microbiological Assoc. | 1977-06-14 |
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Every clearance here is in the API, with alerts when new ones post.