510(k) Report

FDA applicant

Lisca Development AB

Linkoping, SE1 decision1992–19920 recalls

FDA records 1 decision for Lisca Development AB (Linkoping, SE) in 1992: 1 510(k) clearance. All are in product code DPW (Flowmeter, Blood, Cardiovascular). 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, cardiovascular panel, where it files most

How often FDA has decided Lisca Development AB’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Lisca Development AB since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Lisca Development AB 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?

  • DPWFlowmeter, Blood, Cardiovascular1decision

Who builds on its devices?

Later devices cite its devices 2 times; 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.

  • K920844Pim 1.0 Laser Doppler Perfusion ImagerLisca Development AB · 19922cite it

What has FDA decided for it lately?

  • K920844Pim 1.0 Laser Doppler Perfusion ImagerLisca Development AB · 1992

The one decision as Lisca Development AB →