INDIRECT IMMUNOFLUORESCENT ANTIBODY ASSAY— 510(k) K881617
Substantially EquivalentGranbio, Inc.
FDA 510(k) clearance K881617 for INDIRECT IMMUNOFLUORESCENT ANTIBODY ASSAY, Substantially Equivalent on 1988-06-07. Applicant: Granbio, Inc..
Clearance details
- Applicant
- Granbio, Inc.
- Product code
- Code LSE
- Advisory panel
- Microbiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Temecula, CA, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.