510(k) Report

FDA applicant

Intl. Medical Industries

Watertown, MA3 decisions1985–19860 recalls

FDA records 3 decisions for Intl. Medical Industries (Watertown, MA) from 1985 to 1986: 3 510(k) clearances. Most are in product codes LHI (Set, I.V. Fluid Transfer) and FMF (Syringe, Piston). 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 Intl. Medical Industries’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Intl. Medical Industries since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Intl. Medical Industries’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?

  • LHISet, I.V. Fluid Transfer2decisions
  • FMFSyringe, Piston1decision

Who builds on its devices?

Later devices cite its devices 4 times; 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.

  • K861276Tamper Proof CapIntl. Medical Industries · 19864cite it

What has FDA decided for it lately?

  • K861276Tamper Proof CapIntl. Medical Industries · 1986
  • K860434Chemo-VentIntl. Medical Industries · 1986
  • K850051Versa-Fill 120 & Fill Set 42-50Intl. Medical Industries · 1985

All 3 as Intl. Medical Industries →