MetaLite DX 数字病理软件
K号: K240303 · 2024-10-28
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决定日期2024-10-28
产品代码QKQ
咨询委员会PA
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。
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器械摘要
MetaLite DX Digital Pathology Software is the device name listed in this FDA 510(k) record. The listed applicant is Jellox Biotech, Inc.. It received FDA 510(k) clearance on 2024-10-28 under 510(k) number K240303. The device is classified under product code QKQ. It was reviewed by the PA advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the MetaLite DX Digital Pathology Software?
MetaLite DX Digital Pathology Software is a medical device that received FDA 510(k) clearance on 2024-10-28. The listed applicant is Jellox Biotech, Inc.. The 510(k) number is K240303.
When did MetaLite DX Digital Pathology Software receive FDA 510(k) clearance?
MetaLite DX Digital Pathology Software received FDA 510(k) clearance on 2024-10-28, under 510(k) number K240303.
Who is the listed applicant for MetaLite DX Digital Pathology Software?
The FDA 510(k) record lists Jellox Biotech, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MetaLite DX Digital Pathology Software?
The FDA product code for MetaLite DX Digital Pathology Software is QKQ.
相关临床试验
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：QKQ）
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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