HIgH-Flo Super26 皮下针套装
K号: K180843 · 2019-04-04
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器械摘要
常见问题
What is the HIgH-Flo Super26 Subcutaneous Needle Sets?
HIgH-Flo Super26 Subcutaneous Needle Sets is a medical device that received FDA 510(k) clearance on 2019-04-04. The listed applicant is Repro-Med Systems, Inc. Dba Rms Medical Products. The 510(k) number is K180843.
When did HIgH-Flo Super26 Subcutaneous Needle Sets receive FDA 510(k) clearance?
HIgH-Flo Super26 Subcutaneous Needle Sets received FDA 510(k) clearance on 2019-04-04, under 510(k) number K180843.
Who is the listed applicant for HIgH-Flo Super26 Subcutaneous Needle Sets?
The FDA 510(k) record lists Repro-Med Systems, Inc. Dba Rms Medical Products as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for HIgH-Flo Super26 Subcutaneous Needle Sets?
The FDA product code for HIgH-Flo Super26 Subcutaneous Needle Sets is FPA.
相关临床试验
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列明Repro-Med Systems, Inc. Dba Rms Medical Products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:FPA)
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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