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Alltest Multi-Drug Rapid Urine Test Panel

Hangzhou AllTest Biotech Co., Ltd. · Model 1 · UDI-DI 16936983169599

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0
510(k) clearances
0
Adverse events
0
Recalls
52
Facilities

Description

25T/Box, FDA Clia Waived, MOP300/OXY100/PCP25/MET500/MDMA500/MTD300/AMP500/BAR300/BZO300/COC150/THC50/TCA1000/BUP10/FYL1

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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.