23andMe PGS 遗传风险报告 for 遗传性前列腺癌 (HOXB13 相关)
K号: K211499 · 2022-01-06
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器械摘要
常见问题
What is the 23andMe PGS Genetic Risk Report for Hereditary Prostate Cancer (HOXB13-Related)?
23andMe PGS Genetic Risk Report for Hereditary Prostate Cancer (HOXB13-Related) is a medical device that received FDA 510(k) clearance on 2022-01-06. The listed applicant is 23AndMe, Inc.. The 510(k) number is K211499.
When did 23andMe PGS Genetic Risk Report for Hereditary Prostate Cancer (HOXB13-Related) receive FDA 510(k) clearance?
23andMe PGS Genetic Risk Report for Hereditary Prostate Cancer (HOXB13-Related) received FDA 510(k) clearance on 2022-01-06, under 510(k) number K211499.
Who is the listed applicant for 23andMe PGS Genetic Risk Report for Hereditary Prostate Cancer (HOXB13-Related)?
The FDA 510(k) record lists 23AndMe, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for 23andMe PGS Genetic Risk Report for Hereditary Prostate Cancer (HOXB13-Related)?
The FDA product code for 23andMe PGS Genetic Risk Report for Hereditary Prostate Cancer (HOXB13-Related) is QAZ.
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。
列明23AndMe, 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:QAZ)
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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