无菌一次性使用LDV注射器,CHOICARE无菌一次性使用LDV注射器
K号: K213013 · 2022-09-19
广告
器械摘要
常见问题
What is the Sterile Single-use LDV Syringe, CHOICARE Sterile Single-use LDV Syringe?
Sterile Single-use LDV Syringe, CHOICARE Sterile Single-use LDV Syringe is a medical device that received FDA 510(k) clearance on 2022-09-19. The listed applicant is Jeil Tech Co., Ltd.. The 510(k) number is K213013.
When did Sterile Single-use LDV Syringe, CHOICARE Sterile Single-use LDV Syringe receive FDA 510(k) clearance?
Sterile Single-use LDV Syringe, CHOICARE Sterile Single-use LDV Syringe received FDA 510(k) clearance on 2022-09-19, under 510(k) number K213013.
Who is the listed applicant for Sterile Single-use LDV Syringe, CHOICARE Sterile Single-use LDV Syringe?
The FDA 510(k) record lists Jeil Tech Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Sterile Single-use LDV Syringe, CHOICARE Sterile Single-use LDV Syringe?
The FDA product code for Sterile Single-use LDV Syringe, CHOICARE Sterile Single-use LDV Syringe is QNQ.
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。
相关器械(代码:QNQ)
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。
广告