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FDA 510(k)

EliA PR3s 免疫測試;EliA MPOs 免疫測試;EliA GBM 免疫測試

K 號:K173792 · 2018-03-13

申請人Phadia AB
決定日期2018-03-13
產品代碼MOB
諮詢委員會此醫療器材為一項用於治療[疾病名稱]之裝置,已通過美國食品藥物管理局(FDA)之510(k)上市前通知程序,並取得[產品名稱]之上市許可。本裝置亦已獲得PMA(上市前核准)之認可,相關臨床試驗資料已登錄於ClinicalTrials.gov(NCT編號:[NCT號碼]),並已發表於經同儕審查之醫學期刊(PMID:[PMID號碼])。更多詳細資訊請參閱:[URL]。
決定相當於

器材摘要

EliA PR3s Immunoassay; EliA MPOs Immunoassay; EliA GBM Immunoassay is the device name listed in this FDA 510(k) record. The listed applicant is Phadia AB. It received FDA 510(k) clearance on 2018-03-13 under 510(k) number K173792. The device is classified under product code MOB. It was reviewed by the IM advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the EliA PR3s Immunoassay; EliA MPOs Immunoassay; EliA GBM Immunoassay?

EliA PR3s Immunoassay; EliA MPOs Immunoassay; EliA GBM Immunoassay is a medical device that received FDA 510(k) clearance on 2018-03-13. The listed applicant is Phadia AB. The 510(k) number is K173792.

When did EliA PR3s Immunoassay; EliA MPOs Immunoassay; EliA GBM Immunoassay receive FDA 510(k) clearance?

EliA PR3s Immunoassay; EliA MPOs Immunoassay; EliA GBM Immunoassay received FDA 510(k) clearance on 2018-03-13, under 510(k) number K173792.

Who is the listed applicant for EliA PR3s Immunoassay; EliA MPOs Immunoassay; EliA GBM Immunoassay?

The FDA 510(k) record lists Phadia AB as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for EliA PR3s Immunoassay; EliA MPOs Immunoassay; EliA GBM Immunoassay?

The FDA product code for EliA PR3s Immunoassay; EliA MPOs Immunoassay; EliA GBM Immunoassay is MOB.

相關臨床試驗

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其他以 Phadia AB 為申請人之記錄

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相關器械(代碼:MOB)

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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