510(k) Report

FDA applicant

Cord Stick Corp.

Modesto, CA1 decision2003–20030 recalls

FDA records 1 decision for Cord Stick Corp. (Modesto, CA) in 2003: 1 510(k) clearance. All are in product code FMI (Needle, Hypodermic, Single Lumen). 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, general hospital panel, where it files most

How often FDA has decided Cord Stick Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Cord Stick Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Cord Stick Corp.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

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Which product codes does it file in?

  • FMINeedle, Hypodermic, Single Lumen1decision

What has FDA decided for it lately?

  • K031058Cord Stick Multiple Draw SystemCord Stick Corp. · 2003

The one decision as Cord Stick Corp. →