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Rapid Response

BTNX Inc · Model D10.14.1-1V · UDI-DI 00722066004890

NFVPTHNGMNGLNGIPTGNFWNGGNFTNFY
2
510(k) clearances
2
Adverse events
0
Recalls
51
Facilities

Description

One Step 10 Panel DOA Cup (10.14.1) - COC150 AMP500 MET500 THC50 MTD300 MOP2000 OXY100 PCP25 BAR300 BZO300

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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.