Requests that the FDA (1) Publicly Report the Number of C-Arm Fluoroscopic and Angiographic X-Ray System Collisions with Patient Tables and/or Patients Recorded in MAUDE; (2) Assess Whether Such Events Are Fully Reported; and (3) Issue a Regulation or Guidance Requiring Anti-Collision Software on All C-Arm Fluoroscopic and Angiographic X-Ray Systems | Federal Regulations · Congress.wiki

Nonrulemaking

FDA

Open for Comments

FDA-2026-P-6248

Requests that the FDA (1) Publicly Report the Number of C-Arm Fluoroscopic and Angiographic X-Ray System Collisions with Patient Tables and/or Patients Recorded in MAUDE; (2) Assess Whether Such Events Are Fully Reported; and (3) Issue a Regulation or Guidance Requiring Anti-Collision Software on All C-Arm Fluoroscopic and Angiographic X-Ray Systems

Documents

Comments

Description

Open

Key Dates

Comment Period OpensJun 29, 2026

Documents

Type	Title	Posted	Comments	Status
Supporting Material	Page 16 References - Part 2 - Reference 2 - a	Jun 29, 2026	--

Keywords

CDRH

Citizen Petition

Request that the FDA

(1) Publicly Report the Number of

C-Arm Fluoroscopic and

Angiographic X-Ray System Collisions

with Patient Tables and/or Patients Recorded

in MAUDE

Data from Regulations.gov