GRD — Antiserum, Hai, Mumps Virus Class I
FDA product code GRD covers "Antiserum, Hai, Mumps Virus", a Class I medical device regulated under 21 CFR 866.3380. Submissions are reviewed by the Microbiology panel. At least 1 recent 510(k) clearance has been granted under this product code.
Classification Details
- Product Code
- GRD
- 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 |
|---|---|---|---|
| K833077 | wellcome diagnostics | WELLCOGEN H. INFLUENZAL ZL21 | January 10, 1984 |