510(k) Report

FDA applicant

Airborne Life Support Systems, Inc.

Cleburne, TX1 decision1985–19850 recalls

FDA records 1 decision for Airborne Life Support Systems, Inc. (Cleburne, TX) in 1985: 1 510(k) clearance. All are in product code FPL (Incubator, Neonatal Transport). 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 Airborne Life Support Systems, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Airborne Life Support Systems, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Airborne Life Support Systems, Inc. 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?

  • FPLIncubator, Neonatal Transport1decision

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.

  • K850496Transport Incubator 185Airborne Life Support Systems, Inc. · 19852cite it

What has FDA decided for it lately?

  • K850496Transport Incubator 185Airborne Life Support Systems, Inc. · 1985

The one decision as Airborne Life Support Systems, Inc. →