SKR 3000
K号: K182688 · 2018-12-18
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器械摘要
SKR 3000 is the device name listed in this FDA 510(k) record. The listed applicant is Konica Minolta, Inc.. It received FDA 510(k) clearance on 2018-12-18 under 510(k) number K182688. The device is classified under product code MQB. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the SKR 3000?
SKR 3000 is a medical device that received FDA 510(k) clearance on 2018-12-18. The listed applicant is Konica Minolta, Inc.. The 510(k) number is K182688.
When did SKR 3000 receive FDA 510(k) clearance?
SKR 3000 received FDA 510(k) clearance on 2018-12-18, under 510(k) number K182688.
Who is the listed applicant for SKR 3000?
The FDA 510(k) record lists Konica Minolta, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SKR 3000?
The FDA product code for SKR 3000 is MQB.
列明Konica Minolta, 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：MQB）
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。
K2538000909FCE，0909FCE-HSRayence Co., Ltd.K260820VIVIX-S 4386W (FXRD-4386WA)Vieworks Co., Ltd.K252996通用 1417PIKonica Minolta Healthcare Americas, Inc.K252911Lux HD 2530 探测器 (Lux HD 2530)Iray Imaging Technology (Haining) LimitedK250211玉山X射线平板探测器Innocare Optoelectronics Corp.K250665SKR 3000Konica Minolta, Inc.
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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