510(k) Report

FDA applicant

Angiplast Private, Ltd.

Ahmedabad, IN1 decision2002–20020 recalls

FDA records 1 decision for Angiplast Private, Ltd. (Ahmedabad, IN) in 2002: 1 510(k) clearance. All are in product code LHI (Set, I.V. Fluid Transfer). 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 Angiplast Private, Ltd.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Angiplast Private, Ltd. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Angiplast Private, Ltd. 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?

  • LHISet, I.V. Fluid Transfer1decision

Who builds on its devices?

Later devices cite its devices 1 time; 0 of those are its own. The firms that cite it most:

Which of its devices are cited most?

Its devices that later submissions most often claim equivalence to.

  • K012189Angeltouch Vented IV Administration SetAngiplast Private, Ltd. · 20021cites it

What has FDA decided for it lately?

  • K012189Angeltouch Vented IV Administration SetAngiplast Private, Ltd. · 2002

The one decision as Angiplast Private, Ltd. →