510(k) Report

FDA applicant

D&R X-Ray Products, Inc.

Richmond, VA5 decisions1985–19860 recalls

FDA records 5 decisions for D&R X-Ray Products, Inc. (Richmond, VA) from 1985 to 1986: 5 510(k) clearances. Most are in product codes IZW (Collimator, Automatic, Radiographic) and IZZ (Table, Radiographic, Non-Tilting, Powered). 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 D&R X-Ray Products, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for D&R X-Ray Products, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — D&R X-Ray Products, Inc. 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?

  • IZWCollimator, Automatic, Radiographic1decision
  • IZZTable, Radiographic, Non-Tilting, Powered1decision
  • IXRTable, Radiographic, Tilting1decision
  • IZXCollimator, Manual, Radiographic1decision
  • IYBTube Mount, X-Ray, Diagnostic1decision

What has FDA decided for it lately?

  • K862734Ceilstand, Multistand R & S and the BuckystandD&R X-Ray Products, Inc. · 1986
  • K861942Collimator Model A280BLE & Model A280-BLMD&R X-Ray Products, Inc. · 1986
  • K861941Collimator Model A280BLMD & Model A280BLMPD&R X-Ray Products, Inc. · 1986
  • K861940Radiographic Tables Models A71OS-T,A71OT-T,A71OB-TD&R X-Ray Products, Inc. · 1986
  • K850948Tilting Table Radiographic A9006 TomojupiterD&R X-Ray Products, Inc. · 1985

All 5 as D&R X-Ray Products, Inc. →