Rapid Pathogen Screening, Inc. is one of 14110 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Rapid Pathogen Screening, Inc. - FDA 510(k) Cleared Devices
Recent clearances: INFLAMMA DRY, RPS ADENO DETECTOR PLUS
2
Total
2
Cleared
0
Denied
Rapid Pathogen Screening, Inc. has 2 FDA 510(k) cleared medical devices. Based in Sarasota, US.
Historical record: 2 cleared submissions from 2011 to 2013. Primary specialty: Chemistry.
Browse the FDA 510(k) cleared devices submitted by Rapid Pathogen Screening, Inc. Filter by specialty or product code using the sidebar.
1 device has linked clinical trial registered on ClinicalTrials.gov.
FDA 510(k) Regulatory Record - Rapid Pathogen Screening, Inc.
2 devices