510(k) Report

FDA applicant

Cdp, Ltd.

Kiriat Arie, Petach Tikva, IL1 decision2007–20072 recalls

FDA records 1 decision for Cdp, Ltd. (Kiriat Arie, Petach Tikva, IL) in 2007: 1 510(k) clearance. All are in product code LLZ (System, Image Processing, Radiological). Its devices cite 1 predicate, 0 of them its own earlier devices. 2 recalls are linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, radiology panel, where it files most

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

FDA decisions per year

1in 2007

2007: 1
2007high 1 (2007) · low 0 (2008)2026

2026 so far, outlined.

Recalls per year

1in 2014

2011: 12014: 1
2007high 1 (2011) · low 0 (2007)2026

Class I Class II/III not classified

FIG. 1 — Cdp, Ltd. 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?

  • LLZSystem, Image Processing, Radiological1decision

Whose devices does it build on?

Its devices cite 1 predicate; 0 are its own earlier devices. The firms it cites most:

What has FDA decided for it lately?

  • K072960CDP 5000, Media and Distribution Center, DiagnetCdp, Ltd. · 20072 recalls

The one decision as Cdp, Ltd. →

What has been recalled?

2 recalls linked to its devices; the latest:

  • K072960Philips MDC PACS R2.X / IntelliSpace PACS DCX R3.1 software, software application that…Apr 2, 2014Class II
  • K072960MDC PACS - release R2.3 SP1 . Phillips Healthcare Andover, Massachusetts A software…Sep 1, 2011