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Pace Aid
HOME
WHY PACEAID?
  • White Paper - Beta Test
  • An Executive Brief
  • R3 Resuscitation Standard
DETAILS
  • About Us
  • FAQs
  • Gallery
  • BTI Highlights PaceAid
  • Information for Use PDFs
FAQs - More
  • FAQs
  • Terms of Service Policy
  • Privacy Policy
  • Return Policy
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  • HOME
  • WHY PACEAID?
    • White Paper - Beta Test
    • An Executive Brief
    • R3 Resuscitation Standard
  • DETAILS
    • About Us
    • FAQs
    • Gallery
    • BTI Highlights PaceAid
    • Information for Use PDFs
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  • HOME
  • WHY PACEAID?
    • White Paper - Beta Test
    • An Executive Brief
    • R3 Resuscitation Standard
  • DETAILS
    • About Us
    • FAQs
    • Gallery
    • BTI Highlights PaceAid
    • Information for Use PDFs
  • FAQs - More
    • FAQs
    • Terms of Service Policy
    • Privacy Policy
    • Return Policy
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Press Release

PaceAid Launches Visual CPR Guidance Tool

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About Us

Medical trainees practice CPR on a training mannequin.

PaceAid is an innovative visual CPR guidance device created to support the processes of resuscitation.

PaceAid® provides clear, easy‑to‑follow visual cues to help guide bystanders, first responders, and healthcare professionals in performing CPR with greater confidence and consistency during critical moments. PaceAid is intended as a visual guidance tool to support responders when every second matters.  


CPR Guidance When Every Second Counts

The mission of PaceAid® is to provide accessible tools and educational resources that enhance knowledge and skills in accordance with established CPR guidelines. We aim to equip individuals with the confidence to respond in emergencies while ensuring all offerings comply with regulatory standards.   

A Wave of Innovation

PaceAid® was developed by Oceana Medical, a company committed to advancing innovation in healthcare. Our focus is on creating guidance tools that support responders and promote safe, consistent practices during critical moments.     

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PaceAid is a Class 1 medical device registered and listed with the FDA. FDA registration means the manufacturer has provided the required information to the FDA, but the FDA has not reviewed or approved this product for safety or efficacy. PaceAid is manufactured in accordance with current good manufacturing practices (CGMPs). 

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