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VeriCheck Drug Test Cup
Verify Diagnostics Inc · Model 1.0 · UDI-DI 00870266000423
4
510(k) clearances
1
Adverse events
0
Recalls
50
Facilities
Description
AMP1000 COC300 MET1000 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.
