FDA applicant

Eucardio Laboratory, Inc.

San Diego, CA4 decisions1990–19940 recalls

FDA records 4 decisions for Eucardio Laboratory, Inc. (San Diego, CA) from 1990 to 1994: 4 510(k) clearances. Most are in product codes JHI (Visual, Pregnancy Hcg, Prescription Use) and DFC (Lipoprotein, Low-Density, Antigen, Antiserum…). 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 Eucardio Laboratory, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Eucardio Laboratory, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Eucardio Laboratory, Inc.

Which product codes does it file in?

What has FDA decided for it lately?