510(k) Report

FDA applicant

Rf Systems Lab.

Ormond Beach, FL1 decision2006–20060 recalls

FDA records 1 decision for Rf Systems Lab. (Ormond Beach, FL) in 2006: 1 510(k) clearance. All are in product code MQB (Solid State X-Ray Imager (Flat Panel/Digital…). 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, radiology panel, where it files most

How often FDA has decided Rf Systems Lab.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Rf Systems Lab. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Rf Systems Lab.’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?

  • MQBSolid State X-Ray Imager (Flat Panel/Digital Imager)1decision

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.

  • K062376Direct Digital Radiography CCD Imaging Sensor, NaomiRf Systems Lab. · 20061cites it

What has FDA decided for it lately?

  • K062376Direct Digital Radiography CCD Imaging Sensor, NaomiRf Systems Lab. · 2006

The one decision as Rf Systems Lab. →