AVIEW
K号: K200714 · 2020-08-26
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器械摘要
AVIEW is the device name listed in this FDA 510(k) record. The listed applicant is Coreline Soft Co., Ltd.. It received FDA 510(k) clearance on 2020-08-26 under 510(k) number K200714. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the AVIEW?
AVIEW is a medical device that received FDA 510(k) clearance on 2020-08-26. The listed applicant is Coreline Soft Co., Ltd.. The 510(k) number is K200714.
When did AVIEW receive FDA 510(k) clearance?
AVIEW received FDA 510(k) clearance on 2020-08-26, under 510(k) number K200714.
Who is the listed applicant for AVIEW?
The FDA 510(k) record lists Coreline Soft Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for AVIEW?
The FDA product code for AVIEW is LLZ.
相关临床试验
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列明Coreline Soft Co., Ltd.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：LLZ）
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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请注意，由于您没有提供具体的医疗设备监管文本，我无法提供准确的翻译。如果您能提供具体的文本内容，我将能够为您提供准确的翻译。Taiwan Main Orthopaedic Biotechnology Co., Ltd.K261861SPINEsim v1.0Mdsim S.A.K2620603D-RD-SRadiopharmaceutical Imaging & Dosimetry, LLC
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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