implantable pacemaker Pulse-generator
PMA番号：P950037 · 2026-09-25
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医療機器の概要
implantable pacemaker Pulse-generator is the device name listed in this FDA 510(k) record. The listed applicant is Biotronik, Inc.. It received FDA 510(k) clearance on 2026-09-25. The device is classified under product code DXY. It was reviewed by the CV advisory panel. Product code DXY falls under the category of Clinical Chemistry, which covers reagents and instruments for chemical analysis of clinical samples. Devices in this category are subject to specific FDA regulatory requirements.
よくある質問
What is the implantable pacemaker Pulse-generator?
implantable pacemaker Pulse-generator is a medical device that received FDA 510(k) clearance on 2026-09-25. The listed applicant is Biotronik, Inc..
When did implantable pacemaker Pulse-generator receive FDA 510(k) clearance?
The clearance date for implantable pacemaker Pulse-generator can be found in the official FDA records.
Who is the listed applicant for implantable pacemaker Pulse-generator?
The FDA 510(k) record lists Biotronik, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for implantable pacemaker Pulse-generator?
The FDA product code for implantable pacemaker Pulse-generator is DXY. This falls under the Clinical Chemistry 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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