KARL STORZ SUPRALOOP
K号: K254303 · 2026-09-24
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器械摘要
KARL STORZ SUPRALOOP is the device name listed in this FDA 510(k) record. The listed applicant is Karl Storz SE & CO. KG. It received FDA 510(k) clearance on 2026-09-24 under 510(k) number K254303. The device is classified under product code KNF. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the KARL STORZ SUPRALOOP?
KARL STORZ SUPRALOOP is a medical device that received FDA 510(k) clearance on 2026-09-24. The listed applicant is Karl Storz SE & CO. KG. The 510(k) number is K254303.
When did KARL STORZ SUPRALOOP receive FDA 510(k) clearance?
KARL STORZ SUPRALOOP received FDA 510(k) clearance on 2026-09-24, under 510(k) number K254303.
Who is the listed applicant for KARL STORZ SUPRALOOP?
The FDA 510(k) record lists Karl Storz SE & CO. KG as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for KARL STORZ SUPRALOOP?
The FDA product code for KARL STORZ SUPRALOOP is KNF.
相关临床试验
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列明Karl Storz SE & CO. KG为申报人的其他记录
关联记录通过名称、产品代码或其他元数据自动匹配。匹配不意味着已验证临床、科学、企业或监管关系；请查阅链接的官方来源。
K254252UNIDRIVE SIII System; HOPKINS Telescope 0º (26205AMA) Operating Sheath (26205CD) Obturator (26205OC) Shaver Blade (26205SA) Shaver Blade (26205SB) Shaver Blade (091133-01/-10) Shaver Blade (091134-01/-10)K261102UNIDRIVE Select SystemK254299CLEARVISION Irrigation Sheath 0° (7241AS); CLEARVISION Irrigation Sheath 30° (7241BS); CLEARVISION Irrigation Sheath 45° (7241FS)K260884UNIDRIVE Select SystemK254103HOPKINS Telescopes for ArthroscopyK260209ENDOFLATOR+; Smart Smoke Evacuation
相关器械（代码：KNF）
关联记录通过名称、产品代码或其他元数据自动匹配。匹配不意味着已验证临床、科学、企业或监管关系；请查阅链接的官方来源。
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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