SCANLISA HUMAN CRP ELISA KIT— 510(k) K894573
Substantially EquivalentImmuntech A/S
FDA 510(k) clearance K894573 for SCANLISA HUMAN CRP ELISA KIT, Substantially Equivalent on 1989-08-10. Applicant: Immuntech A/S.
Clearance details
- Applicant
- Immuntech A/S
- Product code
- Code DCK
- Advisory panel
- Immunology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Denmark, DK
Data sourced from openFDA. This site is unofficial and independent of the FDA.