尿道前列腺支架，永久或半永久性
PMA编号：P250011 · 2026-09-24
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器械摘要
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.
常见问题
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.
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官方来源
在 FDA 数据库中查看 →数据来源于FDA开放API。如需最新且权威的信息，请务必参考官方记录。
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