FDA applicant

Los Alamos Diagnostics

Los Alamos, NM7 decisions1987–19890 recalls

FDA records 7 decisions for Los Alamos Diagnostics (Los Alamos, NM) from 1987 to 1989: 7 510(k) clearances. Most are in product codes JJQ (Colorimeter, Photometer, Spectrophotometer For…) and JXA (Kit, Screening, Urine). No recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, clinical chemistry panel, where it files most

How often FDA has decided Los Alamos Diagnostics’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Los Alamos Diagnostics since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Los Alamos Diagnostics by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Los Alamos Diagnostics

Which product codes does it file in?

What has FDA decided for it lately?