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Precision DX Multi-Panel Drug Test Card
Hangzhou AllTest Biotech Co., Ltd. · Model 1 · UDI-DI 16936983152447
10
510(k) clearances
34
Adverse events
0
Recalls
52
Facilities
Description
25T, FDA CLIA Waived,COC150/MET500/AMP500/THC50
Query this across every FDA database — by API.
Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
Get your free API keyRead the docsData 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.
