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