510(k) K862630— MYCOPLASMA PNEUMONIAE ANTIBODY LATEX TEST SYSTEM
Substantially EquivalentMedical Diagnostic Technologies, Inc.
Clearance details
- Applicant
- Medical Diagnostic Technologies, Inc.
- Product code
- Code GSA
- Advisory panel
- Microbiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Augusta, GA, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.