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Rapid Response

BTNX Inc · Model D8.25-1P29-25 · UDI-DI 10722066005658

NFTNFYNGGNGLNFVPTHNGMNFW Prescription
10
510(k) clearances
8
Adverse events
0
Recalls
50
Facilities

Description

Rapid Response Drug Test Panel (8.25) AMP1000 BAR300 BZO300 COC300 MET1000 OPI2000 PCP25 THC50. For the detection of drugs in human urine. 25 tests/kit.

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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.