510(k) Report

FDA applicant

Anrad Corp.

Peabody, MA2 decisions2004–20050 recalls

FDA records 2 decisions for Anrad Corp. (Peabody, MA) from 2004 to 2005: 2 510(k) clearances. All are in product code MQB (Solid State X-Ray Imager (Flat Panel/Digital…). Its devices cite 4 predicates, 1 of them its own earlier devices. 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 Anrad Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Anrad Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Anrad Corp.’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)2decisions

Whose devices does it build on?

Its devices cite 4 predicates; 1 are its own earlier devices. The firms it cites most:

Which of its devices are cited most?

Its devices that later submissions most often claim equivalence to.

  • K042821Digital Detector, Model GR17Anrad Corp. · 20041cites it

What has FDA decided for it lately?

  • K052136GR17 Digital DetectorAnrad Corp. · 2005
  • K042821Digital Detector, Model GR17Anrad Corp. · 2004

All 2 as Anrad Corp. →