510(k) Report

FDA applicant

Androsystems Srl

Rome, IT1 decision1999–19990 recalls

FDA records 1 decision for Androsystems Srl (Rome, IT) in 1999: 1 510(k) clearance. All are in product code KZH (Introducer, Syringe Needle). Its devices cite 1 predicate, 0 of them its own earlier devices. 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 Androsystems Srl’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Androsystems Srl since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Androsystems Srl 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?

  • KZHIntroducer, Syringe Needle1decision

Whose devices does it build on?

Its devices cite 1 predicate; 0 are its own earlier devices. The firms it cites most:

What has FDA decided for it lately?

  • K991680SoftinjectAndrosystems Srl · 1999

The one decision as Androsystems Srl →