Catheter, percutaneous, cardiac ablation, for treatment of atrial fibrillation
PMA 번호: P100010 · 2026-09-25
광고
기기 요약
자주 묻는 질문
What is the Catheter, percutaneous, cardiac ablation, for treatment of atrial fibrillation?
Catheter, percutaneous, cardiac ablation, for treatment of atrial fibrillation is a medical device that received FDA 510(k) clearance on 2026-09-25. The listed applicant is Medtronic Cryocath, LP.
When did Catheter, percutaneous, cardiac ablation, for treatment of atrial fibrillation receive FDA 510(k) clearance?
The clearance date for Catheter, percutaneous, cardiac ablation, for treatment of atrial fibrillation can be found in the official FDA records.
Who is the listed applicant for Catheter, percutaneous, cardiac ablation, for treatment of atrial fibrillation?
The FDA 510(k) record lists Medtronic Cryocath, LP as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Catheter, percutaneous, cardiac ablation, for treatment of atrial fibrillation?
The FDA product code for Catheter, percutaneous, cardiac ablation, for treatment of atrial fibrillation is OAE.
관련 임상시험
관련 기록은 이름, 제품 코드 또는 기타 메타데이터를 사용하여 자동으로 매칭됩니다. 매칭은 검증된 임상, 과학, 기업 또는 규제 상의 관계를 입증하지 않으며, 연결된 공식 출처를 검토하시기 바랍니다.
공식 출처
FDA 데이터베이스에서 보기 →FDA Open API에서 수집된 데이터입니다. 가장 정확하고 공인된 정보는 항상 공식 레코드를 참조하시기 바랍니다.
광고