RA LATEX TEST— 510(k) K812972
Substantially EquivalentOxoid U.S.A., Inc.
FDA 510(k) clearance K812972 for RA LATEX TEST, Substantially Equivalent on 1981-11-06. Applicant: Oxoid U.S.A., Inc..
Clearance details
- Applicant
- Oxoid U.S.A., Inc.
- Product code
- Code DHR
- Advisory panel
- Immunology
- 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.