Hem-o-lok® Ligating Clips
K号: K232970 · 2024-01-12
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器械摘要
Hem-o-lok® Ligating Clips is the device name listed in this FDA 510(k) record. The listed applicant is Teleflex Medical. It received FDA 510(k) clearance on 2024-01-12 under 510(k) number K232970. The device is classified under product code FZP. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the Hem-o-lok® Ligating Clips?
Hem-o-lok® Ligating Clips is a medical device that received FDA 510(k) clearance on 2024-01-12. The listed applicant is Teleflex Medical. The 510(k) number is K232970.
When did Hem-o-lok® Ligating Clips receive FDA 510(k) clearance?
Hem-o-lok® Ligating Clips received FDA 510(k) clearance on 2024-01-12, under 510(k) number K232970.
Who is the listed applicant for Hem-o-lok® Ligating Clips?
FDA 510(k)记录显示Teleflex Medical为申请人。这本身并不能确立该设备制造商的身份。
What is the FDA product code for Hem-o-lok® Ligating Clips?
The FDA product code for Hem-o-lok® Ligating Clips is FZP.
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Teleflex 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：FZP）
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。
K260677血管闭合装置（VCD177213P）Vcd Medical S.R.L.K254231Inno-Hook™ 一次性夹子应用器（结扎夹）和 Inno-Hook™ 结扎夹Taiwan Surgical CorporationK253781InnoClip 套管夹应用器Taiwan Surgical CorporationK253903InnoClip 一次性套管夹应用器Taiwan Surgical CorporationK250643一次性聚合物结扎夹Hangzhou Kangji Medical Instrument Co., Ltd.K251054Hem-o-lok™ PurplePlus™ Large Polymer Ligating ClipsTeleflex Medical
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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