GRA
3 FDA 510(k) clearances · Product code
FDA profile
- Official device name
- Antiserum, Fluorescent, Mumps Virus
- Device class
- Class I (low risk)
- Regulation
- 21 CFR 866.3380
- Medical specialty
- Microbiology
Export predicate table (CSV) Shareable report ◉ Watch exports: 3 free/month · reports & watching: free
| Record | Firm | Date |
|---|---|---|
| MUMPS VIRUS (K894624) | Bion Ent., Ltd. | 1989-10-16 |
| ANTIBODY TO MUMPS VIRUS IFA TEST (K822826) | Electro-Nucleonics Laboratories, Inc. | 1982-12-03 |
| VIRAL ANTISERA, FLUORESCEIN LABELED (K770216) | Flow Laboratories, Inc. | 1977-03-01 |
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Every clearance here is in the API, with alerts when new ones post.