FDA applicant

Abco Dealers, Inc.

Mchenry, IL127 decisions1976–19910 recalls

FDA records 127 decisions for Abco Dealers, Inc. (Mchenry, IL) from 1976 to 1991: 127 510(k) clearances. Most are in product codes KOD (Catheter, Urological) and FMF (Syringe, Piston). 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 Abco Dealers, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Abco Dealers, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Abco”

FDA records each applicant name separately; these may or may not be the same firm.

Abco Dist. 2

Abco Dealers, 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?

Other applicant names beginning “Abco”