510(k) Report

FDA applicant

Innovative Design Assoc.

Upper Saddle River, NJ1 decision1999–19990 recalls

FDA records 1 decision for Innovative Design Assoc. (Upper Saddle River, NJ) 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 Innovative Design Assoc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Innovative Design Assoc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Innovative Design Assoc. 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?

  • K990496Anesflow-Dual Drip IV Infusion SetInnovative Design Assoc. · 1999

The one decision as Innovative Design Assoc. →