VascuChek 套件,VascuChek 收发器,VascuChek 外科探头,VascuChek 充电器
K号: K211589 · 2022-01-27
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器械摘要
常见问题
What is the VascuChek Kit, VascuChek Transceiver, VascuChek Surgical Probe, VascuChek Charger?
VascuChek Kit, VascuChek Transceiver, VascuChek Surgical Probe, VascuChek Charger is a medical device that received FDA 510(k) clearance on 2022-01-27. The listed applicant is Remington Medical, Inc.. The 510(k) number is K211589.
When did VascuChek Kit, VascuChek Transceiver, VascuChek Surgical Probe, VascuChek Charger receive FDA 510(k) clearance?
VascuChek Kit, VascuChek Transceiver, VascuChek Surgical Probe, VascuChek Charger received FDA 510(k) clearance on 2022-01-27, under 510(k) number K211589.
Who is the listed applicant for VascuChek Kit, VascuChek Transceiver, VascuChek Surgical Probe, VascuChek Charger?
The FDA 510(k) record lists Remington Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for VascuChek Kit, VascuChek Transceiver, VascuChek Surgical Probe, VascuChek Charger?
The FDA product code for VascuChek Kit, VascuChek Transceiver, VascuChek Surgical Probe, VascuChek Charger is DPW.
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Remington Medical, 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:DPW)
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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