⚗️FDA Classifies Clinical Mass Spectrometry Devices
Medical Devices; Immunology and Microbiology Devices; Classification of the Clinical Mass Spectrometry Microorganism Identification and Differentiation System
Summary
The Food and Drug Administration (FDA, the Agency, or we) is classifying the clinical mass spectrometry microorganism identification and differentiation system into class II (special controls). The special controls that apply to the device type are identified in this order and will be part of the codified language for the clinical mass spectrometry microorganism identification and differentiation system's classification. We are taking this action because we have determined that classifying the device into class II (special controls) will provide a reasonable assurance of safety and effectiveness of the device. We believe this action will also enhance patients' access to beneficial innovative devices, in part by reducing regulatory burdens.
Agencies
- Health and Human Services Department
- Food and Drug Administration
Business Impact
$$ - Med
The classification of the clinical mass spectrometry microorganism identification and differentiation system into class II (special controls) reduces regulatory burdens, thus encouraging innovation and leading to quicker market access for similar devices. This can directly impact business owners and executives in the medical device sector seeking to navigate FDA regulations.