FIAX TEST KIT FOR ANTI-TOXOPLASMA ANTIBO— 510(k) K790464
Substantially EquivalentIntl. Diagnostic Technology
FDA 510(k) clearance K790464 for FIAX TEST KIT FOR ANTI-TOXOPLASMA ANTIBO, Substantially Equivalent on 1979-06-13. Applicant: Intl. Diagnostic Technology.
Clearance details
- Applicant
- Intl. Diagnostic Technology
- Product code
- Code GLZ
- Advisory panel
- Microbiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Mchenry, IL, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.