Automated external defibrillators (non-wearable)
PMA番号：P160026 · 2026-09-24
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医療機器の概要
Automated external defibrillators (non-wearable) is the device name listed in this FDA 510(k) record. The listed applicant is Physio-Control, Inc.. It received FDA 510(k) clearance on 2026-09-24. The device is classified under product code MKJ. It was reviewed by the CV advisory panel. Product code MKJ falls under the category of Dental, which includes dental instruments, materials, and equipment. Devices in this category are subject to specific FDA regulatory requirements.
よくある質問
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.
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公式ソース
FDAデータベースで見る →データはFDA Open APIから取得しています。最新かつ権威ある情報については、常に公式レコードを参照してください。
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