510(k) Report

FDA applicant

Szabocsik and Associates

Chicago, IL3 decisions2005–20060 recalls

FDA records 3 decisions for Szabocsik and Associates (Chicago, IL) from 2005 to 2006: 3 510(k) clearances. Most are in product codes LPN (Accessories, Soft Lens Products) and MRC (Products, Contact Lens Care, Rigid Gas Permeable). 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, ophthalmic panel, where it files most

How often FDA has decided Szabocsik and Associates’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Szabocsik and Associates since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Szabocsik”

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