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ARCHITECT

Abbott Ireland Diagnostics · Model 3P36-01 · UDI-DI 00380740081287

LOK Prescription
0
510(k) clearances
160
Adverse events
1
Recalls
10
Facilities

Description

ARCHITECT AFP Calibrators

Recalls

DateFirmReason
2003-06-12Abbott Laboratories HPD/ADDAFP results obtained when using the 1:101 automated dilution protocol showed an overestimation of AFP of up to 30.5%

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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.