PowerPAK 注射器
K号: K220114 · 2023-01-25
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决定日期2023-01-25
产品代码MEG
咨询委员会医疗设备监管文本翻译如下：
HO
请注意，由于您没有提供具体的医疗设备监管文本内容，以上仅为示例。请提供具体的文本内容以便进行准确的翻译。
决定实质等同
器械摘要
PowerPAK Syringe is the device name listed in this FDA 510(k) record. The listed applicant is Vault Paragon Group, Inc.. It received FDA 510(k) clearance on 2023-01-25 under 510(k) number K220114. The device is classified under product code MEG. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the PowerPAK Syringe?
PowerPAK Syringe is a medical device that received FDA 510(k) clearance on 2023-01-25. The listed applicant is Vault Paragon Group, Inc.. The 510(k) number is K220114.
When did PowerPAK Syringe receive FDA 510(k) clearance?
PowerPAK Syringe received FDA 510(k) clearance on 2023-01-25, under 510(k) number K220114.
Who is the listed applicant for PowerPAK Syringe?
The FDA 510(k) record lists Vault Paragon Group, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PowerPAK Syringe?
The FDA product code for PowerPAK Syringe is MEG.
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Vault Paragon Group, Inc.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：MEG）
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。
K252098PA3X可拆卸安全套筒注射器（带针）（SC-23ED / SD-23ED）Methyl Co., Ltd.K250847蒸汽盾Vault Paragon Group, Inc.K230287SaviSafe 安全设备Suzhou Savicred Biotechnology Co., Ltd.K231165Shina 注射器; Shina 安全注射器Shina Med CorporationK231907Medline 安全胰岛素和TB注射器Medline Industries, LPK223376Monoject Magellan Insulin Safety Syringe 1mL, 31G x 6mm (8881893110); Monoject Magellan Insulin Safety Syringe 0.5mL, 31G x 6mm (8881893150); Monoject Magellan Insulin Safety Syringe 0.3mL, 31G x 6mm (8881893130)Cardinal Health200, LLC
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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