Automated external defibrillators (non-wearable)
PMA Number: P160022 · 2026-10-02
Device Summary
Frequently Asked Questions
What is the Automated external defibrillators (non-wearable)?
Automated external defibrillators (non-wearable) is a medical device that received FDA 510(k) clearance on 2026-10-02. The listed applicant is ZOLL Medical Corporation.
When did Automated external defibrillators (non-wearable) receive FDA 510(k) clearance?
The clearance date for Automated external defibrillators (non-wearable) can be found in the official FDA records.
Who is the listed applicant for Automated external defibrillators (non-wearable)?
The FDA 510(k) record lists ZOLL Medical Corporation as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Automated external defibrillators (non-wearable)?
The FDA product code for Automated external defibrillators (non-wearable) is MKJ. This falls under the Dental category.
Related Clinical Trials
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.