FDA 510(k)

ImmuLisa 高效着絲點抗體 ELISA

K 號：K151559 · 2016-03-11

決定日期2016-03-11

產品代碼LJM

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

ImmuLisa Enhanced Centromere Antibody ELISA is the device name listed in this FDA 510(k) record. The listed applicant is Immco Diagnostics, Inc.. It received FDA 510(k) clearance on 2016-03-11 under 510(k) number K151559. The device is classified under product code LJM. It was reviewed by the IM advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the ImmuLisa Enhanced Centromere Antibody ELISA?

ImmuLisa Enhanced Centromere Antibody ELISA is a medical device that received FDA 510(k) clearance on 2016-03-11. The listed applicant is Immco Diagnostics, Inc.. The 510(k) number is K151559.

When did ImmuLisa Enhanced Centromere Antibody ELISA receive FDA 510(k) clearance?

ImmuLisa Enhanced Centromere Antibody ELISA received FDA 510(k) clearance on 2016-03-11, under 510(k) number K151559.

Who is the listed applicant for ImmuLisa Enhanced Centromere Antibody ELISA?

The FDA 510(k) record lists Immco Diagnostics, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ImmuLisa Enhanced Centromere Antibody ELISA?

The FDA product code for ImmuLisa Enhanced Centromere Antibody ELISA is LJM.

其他以 Immco Diagnostics, 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。

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相關器械（代碼：LJM）

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。

K182353EliA CENP 免疫測定，EliA U1RNP 免疫測定，EliA RNP70 免疫測定Phadia AB

官方來源

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