Automated external defibrillators (non-wearable)
PMA Number: P160026 · 2026-09-24
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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 2026-09-24. The listed applicant is Physio-Control, Inc..
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 Physio-Control, Inc. 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.
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