510(k) Report

FDA applicant

Valnet Medical Corp.

Santa Isabel, PR1 decision1999–19990 recalls

FDA records 1 decision for Valnet Medical Corp. (Santa Isabel, PR) in 1999: 1 510(k) clearance. All are in product code FPA (Set, Administration, Intravascular). 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 Valnet Medical Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Valnet Medical Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Which product codes does it file in?

  • FPASet, Administration, Intravascular1decision

What has FDA decided for it lately?

  • K983411Colorvees IV Set 20 Drops/ML 105, 60 Drops/ML 105, Vented 20 Drops 105, Vented 60 Drops 105Valnet Medical Corp. · 1999

The one decision as Valnet Medical Corp. →