PROTOPATH FACTOR IX ASSAY— 510(k) K834050
Substantially EquivalentAmerican Dade
FDA 510(k) clearance K834050 for PROTOPATH FACTOR IX ASSAY, Substantially Equivalent on 1984-02-04. Applicant: American Dade.
Clearance details
- Applicant
- American Dade
- Product code
- Code GGP
- Advisory panel
- Hematology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Walker, MI, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.