MDI GLIADIN G TEST— 510(k) K002359
Substantially EquivalentMicro Detect, Inc.
FDA 510(k) clearance K002359 for MDI GLIADIN G TEST, Substantially Equivalent on 2000-10-19. Applicant: Micro Detect, Inc..
Clearance details
- Applicant
- Micro Detect, Inc.
- Product code
- Code MST
- Advisory panel
- Immunology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Tustin, CA, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.