ClearRead X射线气胸
K号: K213566 · 2022-03-10
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器械摘要
ClearRead Xray Pneumothorax is the device name listed in this FDA 510(k) record. The listed applicant is Riverain Technologies, Inc.. It received FDA 510(k) clearance on 2022-03-10 under 510(k) number K213566. The device is classified under product code QFM. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the ClearRead Xray Pneumothorax?
ClearRead Xray Pneumothorax is a medical device that received FDA 510(k) clearance on 2022-03-10. The listed applicant is Riverain Technologies, Inc.. The 510(k) number is K213566.
When did ClearRead Xray Pneumothorax receive FDA 510(k) clearance?
ClearRead Xray Pneumothorax received FDA 510(k) clearance on 2022-03-10, under 510(k) number K213566.
Who is the listed applicant for ClearRead Xray Pneumothorax?
The FDA 510(k) record lists Riverain Technologies, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ClearRead Xray Pneumothorax?
The FDA product code for ClearRead Xray Pneumothorax is QFM.
相关临床试验
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列明Riverain Technologies, 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：QFM）
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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