510(k) Report

FDA applicant

Associated Medical Products Co.

Mchenry, IL29 decisions1980–19970 recalls

FDA records 29 decisions for Associated Medical Products Co. (Mchenry, IL) from 1980 to 1997: 29 510(k) clearances. Most are in product codes LDQ (Unnamed device) and FRG (Wrap, Sterilization). 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 Associated Medical Products Co.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Associated Medical Products Co. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Associated”

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