FDA applicant

Davstar California, Inc.

Lawndale, CA1 decision1989–19890 recalls

FDA records 1 decision for Davstar California, Inc. (Lawndale, CA) in 1989: 1 510(k) clearance. All are in product code KEW (Slides, Microscope). 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, pathology panel, where it files most

How often FDA has decided Davstar California, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Davstar California, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Davstar California, Inc.

Which product codes does it file in?

What has FDA decided for it lately?