RABBIT ANTISERUM TO HUMAN KAPPA LIGHT— 510(k) K831904
Substantially EquivalentDako Corp.
FDA 510(k) clearance K831904 for RABBIT ANTISERUM TO HUMAN KAPPA LIGHT, Substantially Equivalent on 1983-07-19. Applicant: Dako Corp.. Device class: 2.
Clearance details
- Applicant
- Dako Corp.
- Product code
- Code DEO
- Device class
- Class 2
- Regulation
- 21 CFR 866.5550
- Advisory panel
- Immunology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Walker, MI, US
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Data sourced from openFDA. This site is unofficial and independent of the FDA.