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N Antiserum to Human Prealbumin

Siemens Healthcare Diagnostics Products GmbH · Model 10446452 · UDI-DI 00842768011399

JZJ
10
510(k) clearances
5
Adverse events
1
Recalls
33
Facilities

Description

Quantitative determination of prealbumin in human serum and plasma on Siemens nephelometry systems

Recalls

DateFirmReason
2005-11-10Abbott Laboratories Diagnostic DivThese specific protein assays are not meeting the 57-day on board stability claim

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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.