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Rapid Response

BTNX Inc · Model D10.22-1P29-25 · UDI-DI 00722066004593

PTHPTGNGLNGGNFYNFWNFVNFT
1
510(k) clearances
0
Adverse events
0
Recalls
51
Facilities

Description

10-Drug Test Panel - 25/kit(10.22) - COC300 AMP1000 MET1000 THC50 MTD300 MOP300 OXY100 BAR300 BZO300 BUP10

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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.