ANTISERUM TO HUMAN IGM— 510(k) K790705
UnknownKent Laboratories, Inc.
FDA 510(k) clearance K790705 for ANTISERUM TO HUMAN IGM, Unknown on 1979-04-12. Applicant: Kent Laboratories, Inc..
Clearance details
- Applicant
- Kent Laboratories, Inc.
- Product code
- Code DAO
- Advisory panel
- Immunology
- Date received
- Decision date
- Decision
- Unknown
- Clearance type
- Traditional
- Location
- Mchenry, IL, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.