TRANSFORMED PRIMARY HUMAN EMBRYONAL KIDNEY— 510(k) K936171
Substantially EquivalentAdvanced Clinical Diagnostics
FDA 510(k) clearance K936171 for TRANSFORMED PRIMARY HUMAN EMBRYONAL KIDNEY, Substantially Equivalent on 1994-02-03. Applicant: Advanced Clinical Diagnostics.
Clearance details
- Applicant
- Advanced Clinical Diagnostics
- Product code
- Code KIR
- Advisory panel
- Hematology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Toledo, OH, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.