510(k) Report

FDA applicant

Hans-Juergen Huchel

Chicago, IL1 decision1988–19880 recalls

FDA records 1 decision for Hans-Juergen Huchel (Chicago, IL) in 1988: 1 510(k) clearance. All are in product code IRT (Pad, Heating, Powered). 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, physical medicine panel, where it files most

How often FDA has decided Hans-Juergen Huchel’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Hans-Juergen Huchel since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Which product codes does it file in?

  • IRTPad, Heating, Powered1decision

What has FDA decided for it lately?

  • K873576Huchel BodylinerHans-Juergen Huchel · 1988

The one decision as Hans-Juergen Huchel →

Other applicant names beginning “Hans-Juergen”

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

Hans Rudolph, Inc. 11Hans Biomed Corporation 9Hans Hermann GmbH 2Hans J. Brouwers & Assoc. 2Hans Gevder 1