510(k) Report

FDA applicant

Abco Dist.

Mchenry, IL2 decisions1982–19820 recalls

FDA records 2 decisions for Abco Dist. (Mchenry, IL) in 1982: 2 510(k) clearances. Most are in product codes FSM (Tray, Surgical, Instrument) and ETD (Tube, Tympanostomy). 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 Abco Dist.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Abco Dist. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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

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Other applicant names beginning “Abco”

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