STENT, URETHRAL, PROSTATIC, PERMANENT OR SEMI-PERMANENT
PMA 번호: P250011 · 2026-09-24
광고
기기 요약
STENT, URETHRAL, PROSTATIC, PERMANENT OR SEMI-PERMANENT is the device name listed in this FDA 510(k) record. The listed applicant is Proverum, Ltd.. It received FDA 510(k) clearance on 2026-09-24. The device is classified under product code MER. It was reviewed by the GU advisory panel.
자주 묻는 질문
What is the STENT, URETHRAL, PROSTATIC, PERMANENT OR SEMI-PERMANENT?
STENT, URETHRAL, PROSTATIC, PERMANENT OR SEMI-PERMANENT is a medical device that received FDA 510(k) clearance on 2026-09-24. The listed applicant is Proverum, Ltd..
When did STENT, URETHRAL, PROSTATIC, PERMANENT OR SEMI-PERMANENT receive FDA 510(k) clearance?
The clearance date for STENT, URETHRAL, PROSTATIC, PERMANENT OR SEMI-PERMANENT can be found in the official FDA records.
Who is the listed applicant for STENT, URETHRAL, PROSTATIC, PERMANENT OR SEMI-PERMANENT?
The FDA 510(k) record lists Proverum, Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for STENT, URETHRAL, PROSTATIC, PERMANENT OR SEMI-PERMANENT?
The FDA product code for STENT, URETHRAL, PROSTATIC, PERMANENT OR SEMI-PERMANENT is MER.
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.
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공식 출처
FDA 데이터베이스에서 보기 →FDA Open API에서 수집된 데이터입니다. 가장 정확하고 공인된 정보는 항상 공식 레코드를 참조하시기 바랍니다.
광고