Rapid Response
BTNX Inc · Model COF-19CGHU4 · UDI-DI 10722066009618
10
510(k) clearances
53
Adverse events
0
Recalls
30
Facilities
Description
Rapid Response Influenza AB + COVID-19 Antigen Detection Test (Anterior Nasal Swab)
Query this across every FDA database — by API.
Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
Get your free API keyRead the docsData compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.