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FDA Questions for Panel Members: The reclassification process for down-classifying a device from Class III to Class II depends on being able to mitigate the risks associated with use of the diagnostic device such that th
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IndustryTerm
diagnostic device /
/
MedicalCondition
tuberculosis infection /
M. tuberculosis /
tuberculosis /
/
MedicalTreatment
antibiotics /
/
Organization
FDA /
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SocialTag
Tuberculosis
Health in India
Food and Drug Administration
Antibiotic resistance
Mycobacterium tuberculosis
Health
Medicine
Bacteria