510(k) Report

FDA applicant

Ram Development

Israel, IL2 decisions1986–19860 recalls

FDA records 2 decisions for Ram Development (Israel, IL) in 1986: 2 510(k) clearances. Most are in product codes FMG (Stopcock, I.V. Set) and HDR (Cap, Cervical). 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 Ram Development’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Ram Development since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Ram Development 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?

  • FMGStopcock, I.V. Set1decision
  • HDRCap, Cervical1decision

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.

  • K862691StopcockRam Development · 19861cites it

What has FDA decided for it lately?

  • K861305Intrauterine CatheterRam Development · 1986
  • K862691StopcockRam Development · 1986

All 2 as Ram Development →