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Please reach us at info@paceaid.com if you cannot find an answer to your question.
PaceAid is a single‑patient‑use CPR pacing device that provides clear visual cues to help anyone, clinicians, first responders, or bystanders, deliver consistent, guideline‑aligned chest compressions during cardiac arrest.
PaceAid is designed for any environment where CPR may be needed, including:
It supports both trained professionals and lay responders by simplifying CPR pacing.
Activation is intentionally simple:
No. PaceAid is a single‑patient‑use device. This ensures reliability, eliminates reprocessing, and supports infection‑control standards across all environments.
No formal training is required. The device is intuitive and designed to support both trained and untrained responders. It can also be used during CPR classes, drills, and mock codes to reinforce pacing skills.
PaceAid is typically placed on the patient’s chest in a visible location so the person(s) performing compressions and rescue breaths can easily follow the pacing cues.
No. PaceAid is a support tool that helps maintain proper compression rate. It does not replace CPR certification, clinical decision‑making, or established emergency protocols.
Yes. PaceAid is compatible with standard emergency response workflows and can be used alongside AEDs, bag‑valve masks, and other resuscitation tools.
Maintaining the correct compression rate is critical for effective blood flow during cardiac arrest. PaceAid helps reduce variability, especially in high‑stress situations or when responders rotate.
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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