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Rapid Response

BTNX Inc · Model D5.1.1-2FC1E · UDI-DI 10722066006617

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0
510(k) clearances
1
Adverse events
0
Recalls
25
Facilities

Description

Rapid Response 5 Panel Saliva Test Cup E/I Screening (D5.1.1-2FC1E)-THC40 COC20 AMP50 MET50 OPI40. For employment and insurance testing.

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Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

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Data 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.