ENFit 肠内泵注射器 PENTA ENFit,ENFit 肠内泵注射器 NUTRIFIT
K号: K161141 · 2017-03-22
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器械摘要
常见问题
What is the ENFit Enteral Pump Syringes PENTA ENFit, ENFit Enteral Pump Syringes NUTRIFIT?
ENFit Enteral Pump Syringes PENTA ENFit, ENFit Enteral Pump Syringes NUTRIFIT is a medical device that received FDA 510(k) clearance on 2017-03-22. The listed applicant is Pentaferte Italia S.R.L.. The 510(k) number is K161141.
When did ENFit Enteral Pump Syringes PENTA ENFit, ENFit Enteral Pump Syringes NUTRIFIT receive FDA 510(k) clearance?
ENFit Enteral Pump Syringes PENTA ENFit, ENFit Enteral Pump Syringes NUTRIFIT received FDA 510(k) clearance on 2017-03-22, under 510(k) number K161141.
Who is the listed applicant for ENFit Enteral Pump Syringes PENTA ENFit, ENFit Enteral Pump Syringes NUTRIFIT?
The FDA 510(k) record lists Pentaferte Italia S.R.L. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ENFit Enteral Pump Syringes PENTA ENFit, ENFit Enteral Pump Syringes NUTRIFIT?
The FDA product code for ENFit Enteral Pump Syringes PENTA ENFit, ENFit Enteral Pump Syringes NUTRIFIT is PNR.
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Pentaferte Italia S.R.L.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:PNR)
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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