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ProScreen

Instant Tech Subsidiary Acquisition · Model PSD-10CMO3 · UDI-DI 00858998006944

DJC LCM DIS JXM LDJ DIO DJG DKZ LAF Prescription

510(k) clearances

Adverse events

Recalls

Facilities

Description

Drugs of Abuse Test Card, (BZO/BAR)+(OXY/MDMA)+(PCP/AMP)+COC150+MET500+OPI300+THC

Query this across every FDA database — by API.

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.