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VeriCheck Drug Test Cup
Verify Diagnostics Inc · Model 1.0 · UDI-DI 00870266000461
0
510(k) clearances
2
Adverse events
0
Recalls
49
Facilities
Description
AMP500 COC150 MET500 MDMA500 OPI2000 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.
