ScannerSide DoseCheck
K号: K171261 · 2017-08-18
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器械摘要
ScannerSide DoseCheck is the device name listed in this FDA 510(k) record. The listed applicant is Right Dose, Inc.. It received FDA 510(k) clearance on 2017-08-18 under 510(k) number K171261. The device is classified under product code JAK. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the ScannerSide DoseCheck?
ScannerSide DoseCheck is a medical device that received FDA 510(k) clearance on 2017-08-18. The listed applicant is Right Dose, Inc.. The 510(k) number is K171261.
When did ScannerSide DoseCheck receive FDA 510(k) clearance?
ScannerSide DoseCheck received FDA 510(k) clearance on 2017-08-18, under 510(k) number K171261.
Who is the listed applicant for ScannerSide DoseCheck?
The FDA 510(k) record lists Right Dose, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ScannerSide DoseCheck?
The FDA product code for ScannerSide DoseCheck is JAK.
相关临床试验
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相关器械（代码：JAK）
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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