510(k) Report

FDA applicant

Intl. Medical Technologies, Inc.

Mchenry, IL5 decisions1984–19840 recalls

FDA records 5 decisions for Intl. Medical Technologies, Inc. (Mchenry, IL) in 1984: 5 510(k) clearances. Most are in product codes HHI (System, Abortion, Vacuum) and HHM (Sound, Uterine). 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, obstetrics and gynecology panel, where it files most

How often FDA has decided Intl. Medical Technologies, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Intl. Medical Technologies, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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

See the 510(k) Report

Which product codes does it file in?

  • HHISystem, Abortion, Vacuum4decisions
  • HHMSound, Uterine1decision

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.

  • K840383Menstrual Aspiration KitIntl. Medical Technologies, Inc. · 19841cites it

What has FDA decided for it lately?

  • K840382Vacuum Aspiration CatheterIntl. Medical Technologies, Inc. · 1984
  • K840383Menstrual Aspiration KitIntl. Medical Technologies, Inc. · 1984
  • K840381Tapered Cervical DilatorIntl. Medical Technologies, Inc. · 1984
  • K840380Uterine SoundIntl. Medical Technologies, Inc. · 1984
  • K840384Diagnostic Dilatation & Menstrual KitIntl. Medical Technologies, Inc. · 1984

All 5 as Intl. Medical Technologies, Inc. →