FDA applicant

Air-Shields Vickers, Inc.

Hatboro, PA9 decisions1988–19950 recalls

FDA records 9 decisions for Air-Shields Vickers, Inc. (Hatboro, PA) from 1988 to 1995: 9 510(k) clearances. Most are in product codes FMZ (Incubator, Neonatal) and HFM (Monitor, Uterine Contraction, External (For…). 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 Air-Shields Vickers, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Air-Shields Vickers, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Air-Shields Vickers, Inc. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Air-Shields Vickers, Inc.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

See the 510(k) Report

Air-Shields Vickers, Inc.

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?