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FDA 510(k)

ImmunoCAP過敏原w1,普通蒿;ImmunoCAP特定IgE

K 號:K163370 · 2017-05-05

申請人Phadia AB
決定日期2017-05-05
產品代碼DHB
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

ImmunoCAP Allergen w1, Common ragweed; ImmunoCAP Specific IgE is the device name listed in this FDA 510(k) record. The listed applicant is Phadia AB. It received FDA 510(k) clearance on 2017-05-05 under 510(k) number K163370. The device is classified under product code DHB. It was reviewed by the IM advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the ImmunoCAP Allergen w1, Common ragweed; ImmunoCAP Specific IgE?

ImmunoCAP Allergen w1, Common ragweed; ImmunoCAP Specific IgE is a medical device that received FDA 510(k) clearance on 2017-05-05. The listed applicant is Phadia AB. The 510(k) number is K163370.

When did ImmunoCAP Allergen w1, Common ragweed; ImmunoCAP Specific IgE receive FDA 510(k) clearance?

ImmunoCAP Allergen w1, Common ragweed; ImmunoCAP Specific IgE received FDA 510(k) clearance on 2017-05-05, under 510(k) number K163370.

Who is the listed applicant for ImmunoCAP Allergen w1, Common ragweed; ImmunoCAP Specific IgE?

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 ImmunoCAP Allergen w1, Common ragweed; ImmunoCAP Specific IgE?

The FDA product code for ImmunoCAP Allergen w1, Common ragweed; ImmunoCAP Specific IgE is DHB.

相關臨床試驗

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。

其他以 Phadia AB 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。

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相關器械(代碼:DHB)

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。

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