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CHEMTRON BIOTECH INC · Model 712J09A-G · UDI-DI 00812203030209

DNK JXN DKZ JXM DIS DIO DJC DJR LCM LDJ Prescription

510(k) clearances

Adverse events

Recalls

Facilities

Description

10-Panel DOA Cup, AMP/BAR/BZO/COC/MET/MTD/OPI300/PCP/PPX/THC(Cr/SG/Bl)

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.