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FDA 510(k)

23andMe Personal Genome Service (PGS) Pharmacogenetic Reports

K 號:K193492 · 2020-08-17

申請人23AndMe, Inc.
決定日期2020-08-17
產品代碼QDJ
諮詢委員會MG (請提供完整的英文描述,以便進行翻譯。)
決定相當於

器材摘要

23andMe Personal Genome Service (PGS) Pharmacogenetic Reports is the device name listed in this FDA 510(k) record. The listed applicant is 23AndMe, Inc.. It received FDA 510(k) clearance on 2020-08-17 under 510(k) number K193492. The device is classified under product code QDJ. It was reviewed by the MG advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the 23andMe Personal Genome Service (PGS) Pharmacogenetic Reports?

23andMe Personal Genome Service (PGS) Pharmacogenetic Reports is a medical device that received FDA 510(k) clearance on 2020-08-17. The listed applicant is 23AndMe, Inc.. The 510(k) number is K193492.

When did 23andMe Personal Genome Service (PGS) Pharmacogenetic Reports receive FDA 510(k) clearance?

23andMe Personal Genome Service (PGS) Pharmacogenetic Reports received FDA 510(k) clearance on 2020-08-17, under 510(k) number K193492.

Who is the listed applicant for 23andMe Personal Genome Service (PGS) Pharmacogenetic Reports?

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 Personal Genome Service (PGS) Pharmacogenetic Reports?

The FDA product code for 23andMe Personal Genome Service (PGS) Pharmacogenetic Reports is QDJ.

相關臨床試驗

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其他以 23AndMe, Inc. 為申請人之記錄

相關紀錄係使用名稱、產品代碼或其他後設資料自動配對。配對結果並不構成已驗證的臨床、科學、企業或監管關係,請查閱連結的官方來源。

相關器械(代碼:QDJ)

相關紀錄係使用名稱、產品代碼或其他後設資料自動配對。配對結果並不構成已驗證的臨床、科學、企業或監管關係,請查閱連結的官方來源。

官方來源

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