CDT CYTOTOXI TEST— 510(k) K883560
Substantially EquivalentAdvanced Clinical Diagnostics
FDA 510(k) clearance K883560 for CDT CYTOTOXI TEST, Substantially Equivalent on 1988-10-25. Applicant: Advanced Clinical Diagnostics.
Clearance details
- Applicant
- Advanced Clinical Diagnostics
- Product code
- Code LLH
- Advisory panel
- Microbiology
- 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.