Hem-o-lok™ PurplePlus™ Large Polymer Ligating Clips
K号: K251054 · 2025-07-03
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器械摘要
Hem-o-lok™ PurplePlus™ Large Polymer 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 2025-07-03 under 510(k) number K251054. 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™ PurplePlus™ Large Polymer Ligating Clips?
Hem-o-lok™ PurplePlus™ Large Polymer Ligating Clips is a medical device that received FDA 510(k) clearance on 2025-07-03. The listed applicant is Teleflex Medical. The 510(k) number is K251054.
When did Hem-o-lok™ PurplePlus™ Large Polymer Ligating Clips receive FDA 510(k) clearance?
Hem-o-lok™ PurplePlus™ Large Polymer Ligating Clips received FDA 510(k) clearance on 2025-07-03, under 510(k) number K251054.
Who is the listed applicant for Hem-o-lok™ PurplePlus™ Large Polymer 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™ PurplePlus™ Large Polymer Ligating Clips?
The FDA product code for Hem-o-lok™ PurplePlus™ Large Polymer 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。
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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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