---
bio: I am a certified medical device professional with over 30 years experience. I
  have successfully achieved almost 70 FDA 510(k) clearances and 1 EUA during the
  pandemic. Some of the projects I have worked during my career have been trans-myocardial
  revascularization of the heart with a laser, orthopedic, urological, gastro-endoscopic,
  laparoscopic, dermatology & ENT laser systems, a surgical robotics system, an in-home
  kidney dialysis system, an ultrasonic ablation system for neurosurgery, a family
  of trans-jugular liver & percutaneous biopsy devices, catheters, spirometers, Specialty
  Needles (Brachytherapy, Ophthalmic, Suture, Tuohy, & Bone Marrow Biopsy), gastro-enteric
  feeding tubes, an intraoperative MRI system, a neonatal MRI system, SaMD-point of
  care ultrasound imaging of the heart using Artificial Intelligence, Emergency Medical
  Devices (a battlefield chest tube, a wound drainage device, suction Yankauers, wound
  clot dressings, a de-choking device, and an endo-trach placement device), as well
  as class 3 device implants. I am intrigued and passionate about medical device technology
  and its ability to help patients.
hire_date: '2024-07-10'
hobbies: ''
linkedin: null
name: George Hattub
photo: /img/people/George_Hattub-d26bce24c8ad4d108520c55ad8863bcb.jpg
skills: Regulatory Strategy, 510(k) Submissions, Q-SUBs, Due Diligence Audits, Negotiations
testimonials: []
title: Senior Regulatory Affairs Project Manager
---