510(k) Report

FDA applicant

Medoc Corp.

Eilat, IL1 decision1993–19930 recalls

FDA records 1 decision for Medoc Corp. (Eilat, IL) in 1993: 1 510(k) clearance. All are in product code LQW (Test, Temperature Discrimination). 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, neurology panel, where it files most

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

FDA decisions per year

No FDA decision for Medoc Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Medoc Corp. 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?

  • LQWTest, Temperature Discrimination1decision

Who builds on its devices?

Later devices cite its devices 1 time; 0 of those are its own. The firms that cite it most:

Which of its devices are cited most?

Its devices that later submissions most often claim equivalence to.

  • K922052Tsa 2001 Thermal Sensory AnalyzerMedoc Corp. · 19931cites it

What has FDA decided for it lately?

  • K922052Tsa 2001 Thermal Sensory AnalyzerMedoc Corp. · 1993

The one decision as Medoc Corp. →

Other applicant names beginning “Medoc”

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

Medoc Ltd. Advanced Medical Systems 4