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ProScreen

Instant Tech Subsidiary Acquisition · Model PSCupA-7MD-W · UDI-DI 00858998006616

LCMDIOLDJDJGLAFDKZDJC Prescription
1
510(k) clearances
5
Adverse events
1
Recalls
95
Facilities

Description

Drugs of Abuse Cup, CLIA Waived, AMP/COC/MDMA/MET1000/OPI2000/PCP/THC with Cr, Ni, pH, Bl, S.G.

Recalls

DateFirmReason
2005-05-31Applied Biotech IncThe firm has discovered that a number of distributed devices of the Medplus ER Drug Screen Test may be incorrectly assembled which may give incorrect results. The product is an in

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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.