BIOK7600 平板探测器
K号: K190311 · 2019-03-13
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器械摘要
BIOK7600 Flat Panel Detector is the device name listed in this FDA 510(k) record. The listed applicant is Biokinemetrics, Inc.. It received FDA 510(k) clearance on 2019-03-13 under 510(k) number K190311. 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 BIOK7600 Flat Panel Detector?
BIOK7600 Flat Panel Detector is a medical device that received FDA 510(k) clearance on 2019-03-13. The listed applicant is Biokinemetrics, Inc.. The 510(k) number is K190311.
When did BIOK7600 Flat Panel Detector receive FDA 510(k) clearance?
BIOK7600 Flat Panel Detector received FDA 510(k) clearance on 2019-03-13, under 510(k) number K190311.
Who is the listed applicant for BIOK7600 Flat Panel Detector?
The FDA 510(k) record lists Biokinemetrics, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BIOK7600 Flat Panel Detector?
The FDA product code for BIOK7600 Flat Panel Detector is MQB.
相关临床试验
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列明Biokinemetrics, 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。
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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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