EIA KIT FOR THE DETECTION OF GBM ANTIBODIES— 510(k) K953495
Substantially EquivalentScimedx Corp.
FDA 510(k) clearance K953495 for EIA KIT FOR THE DETECTION OF GBM ANTIBODIES, Substantially Equivalent on 1996-04-10. Applicant: Scimedx Corp..
Clearance details
- Applicant
- Scimedx Corp.
- Product code
- Code DBL
- Advisory panel
- Immunology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Denvill, NJ, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.