23AndMe, Inc.
FDA 510(k) & PMA Approved 器材 — 5 products
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器材總數5
類別0
最新 FDA 裁決
| 類型 | 編號 | 器材名稱 | 代碼 | 日期 | 操作 |
|---|---|---|---|---|---|
| 510(k) | K223597 | 23andMe® Personal Genome Service® (PGS®) Genetic Health Risk Report for BRCA1/BRCA2 (Selected Variants) | QAZ | 2023-08-31 | 查看 |
| 510(k) | K221885 | 23andMe Personal Genome Service (PGS) Pharmacogenetic Reports | QDJ | 2022-10-26 | 查看 |
| 510(k) | K211499 | 23andMe PGS Genetic Risk Report for Hereditary Prostate Cancer (HOXB13-Related) | QAZ | 2022-01-06 | 查看 |
| 510(k) | K193492 | 23andMe Personal Genome Service (PGS) Pharmacogenetic Reports | QDJ | 2020-08-17 | 查看 |
| 510(k) | K182784 | MUTYH 相關多腫瘤症(MAP) | QAZ | 2019-01-18 | 查看 |
沒有符合的裝置。