FDA applicant

Pac-Kit Safety Equipment Co.

Mchenry, IL4 decisions1983–19830 recalls

FDA records 4 decisions for Pac-Kit Safety Equipment Co. (Mchenry, IL) in 1983: 4 510(k) clearances. Most are in product codes NAB (Gauze / Sponge,Nonresorbable For External Use) and NAD (Dressing, Wound, Occlusive). 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 and plastic surgery panel, where it files most

How often FDA has decided Pac-Kit Safety Equipment Co.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Pac-Kit Safety Equipment Co. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Pac-Kit Safety Equipment Co. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Pac-Kit Safety Equipment Co.

Which product codes does it file in?

What has FDA decided for it lately?