AK 98 血液透析机,U9000 超滤器,C705 扩展室附件
K号: K201809 · 2021-03-10
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器械摘要
常见问题
What is the AK 98 Dialysis Machine, U9000 Ultrafilter, C705 Expansion Chamber Accessory?
AK 98 Dialysis Machine, U9000 Ultrafilter, C705 Expansion Chamber Accessory is a medical device that received FDA 510(k) clearance on 2021-03-10. The listed applicant is Baxter Healthcare Corportation. The 510(k) number is K201809.
When did AK 98 Dialysis Machine, U9000 Ultrafilter, C705 Expansion Chamber Accessory receive FDA 510(k) clearance?
AK 98 Dialysis Machine, U9000 Ultrafilter, C705 Expansion Chamber Accessory received FDA 510(k) clearance on 2021-03-10, under 510(k) number K201809.
Who is the listed applicant for AK 98 Dialysis Machine, U9000 Ultrafilter, C705 Expansion Chamber Accessory?
The FDA 510(k) record lists Baxter Healthcare Corportation as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for AK 98 Dialysis Machine, U9000 Ultrafilter, C705 Expansion Chamber Accessory?
The FDA product code for AK 98 Dialysis Machine, U9000 Ultrafilter, C705 Expansion Chamber Accessory is KDI.
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列明Baxter Healthcare Corportation为申报人的其他记录
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相关器械(代码:KDI)
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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