N-ASSAY TIA C1-INACTIVATOR TEST KIT— 510(k) K965024
Substantially EquivalentCrestat Diagnostics, Inc.
FDA 510(k) clearance K965024 for N-ASSAY TIA C1-INACTIVATOR TEST KIT, Substantially Equivalent on 1997-07-14. Applicant: Crestat Diagnostics, Inc..
Clearance details
- Applicant
- Crestat Diagnostics, Inc.
- Product code
- Code DBA
- Advisory panel
- Immunology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Weston, CT, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.