Maverix Cryo Biopsy Probe (MCB1000);Maverix Cryo Cartridge (CC1000)
K号: K261068 · 2026-06-30
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器械摘要
常见问题
What is the Maverix Cryo Biopsy Probe (MCB1000);Maverix Cryo Cartridge (CC1000)?
Maverix Cryo Biopsy Probe (MCB1000);Maverix Cryo Cartridge (CC1000) is a medical device that received FDA 510(k) clearance on 2026-06-30. The listed applicant is Serpex Medical. The 510(k) number is K261068.
When did Maverix Cryo Biopsy Probe (MCB1000);Maverix Cryo Cartridge (CC1000) receive FDA 510(k) clearance?
Maverix Cryo Biopsy Probe (MCB1000);Maverix Cryo Cartridge (CC1000) received FDA 510(k) clearance on 2026-06-30, under 510(k) number K261068.
Who is the listed applicant for Maverix Cryo Biopsy Probe (MCB1000);Maverix Cryo Cartridge (CC1000)?
FDA 510(k)记录显示Serpex Medical为申请人。这本身并不足以确立该设备制造商的身份。
What is the FDA product code for Maverix Cryo Biopsy Probe (MCB1000);Maverix Cryo Cartridge (CC1000)?
The FDA product code for Maverix Cryo Biopsy Probe (MCB1000);Maverix Cryo Cartridge (CC1000) is GEH.
相关临床试验
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。
列明Serpex Medical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。
相关器械(代码:GEH)
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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