CuattroDR
K号: K161937 · 2016-10-06
广告
器械摘要
CuattroDR is the device name listed in this FDA 510(k) record. The listed applicant is Cuattro, LLC. It received FDA 510(k) clearance on 2016-10-06 under 510(k) number K161937. The device is classified under product code KPR. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the CuattroDR?
CuattroDR is a medical device that received FDA 510(k) clearance on 2016-10-06. The listed applicant is Cuattro, LLC. The 510(k) number is K161937.
When did CuattroDR receive FDA 510(k) clearance?
CuattroDR received FDA 510(k) clearance on 2016-10-06, under 510(k) number K161937.
Who is the listed applicant for CuattroDR?
The FDA 510(k) record lists Cuattro, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CuattroDR?
The FDA product code for CuattroDR is KPR.
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。
相关器械（代码：KPR）
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。
K260227EXSYS DEXi（EXSYS DEXi-S40S）；EXSYS DEXi（EXSYS DEXi-S40P）；EXSYS DEXi（EXSYS DEXi-S40T）；EXSYS DEXi（EXSYS DEXi-S50H）DRTECH CorporationK260488MULTIX Impact；MULTIX Impact CSiemens Medical Solutions USA, Inc.K260481GC85ASamsung Electronics Co., Ltd.K260482DRE DuoJpi Healthcare Co, Ltd.K253446AeroDR TX c02Dk Medical Systems Co., Ltd.K250954DRX-Evolution Plus X射线系统，DRX-Compass 移动X射线系统，Lux HD 35探测器，Lux HD 43探测器Carestream Health
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。
广告