FDA 510(k)

ZEUS ELISA Borrelia VlsE1/pepC10 IgG/IgM 測試系統；ZEUS ELISA Borrelia burgdorferi IgM 測試系統

K 號：K191240 · 2019-07-29

決定日期2019-07-29

產品代碼LSR

諮詢委員會MI (請提供完整的描述文本，以便進行翻譯。)

決定相當於

器材摘要

ZEUS ELISA Borrelia VlsE1/pepC10 IgG/IgM Test System; ZEUS ELISA Borrelia burgdorferi IgM Test System is the device name listed in this FDA 510(k) record. The listed applicant is Zeus Scientific, Inc.. It received FDA 510(k) clearance on 2019-07-29 under 510(k) number K191240. The device is classified under product code LSR. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the ZEUS ELISA Borrelia VlsE1/pepC10 IgG/IgM Test System; ZEUS ELISA Borrelia burgdorferi IgM Test System?

ZEUS ELISA Borrelia VlsE1/pepC10 IgG/IgM Test System; ZEUS ELISA Borrelia burgdorferi IgM Test System is a medical device that received FDA 510(k) clearance on 2019-07-29. The listed applicant is Zeus Scientific, Inc.. The 510(k) number is K191240.

When did ZEUS ELISA Borrelia VlsE1/pepC10 IgG/IgM Test System; ZEUS ELISA Borrelia burgdorferi IgM Test System receive FDA 510(k) clearance?

ZEUS ELISA Borrelia VlsE1/pepC10 IgG/IgM Test System; ZEUS ELISA Borrelia burgdorferi IgM Test System received FDA 510(k) clearance on 2019-07-29, under 510(k) number K191240.

Who is the listed applicant for ZEUS ELISA Borrelia VlsE1/pepC10 IgG/IgM Test System; ZEUS ELISA Borrelia burgdorferi IgM Test System?

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

What is the FDA product code for ZEUS ELISA Borrelia VlsE1/pepC10 IgG/IgM Test System; ZEUS ELISA Borrelia burgdorferi IgM Test System?

The FDA product code for ZEUS ELISA Borrelia VlsE1/pepC10 IgG/IgM Test System; ZEUS ELISA Borrelia burgdorferi IgM Test System is LSR.

其他以 Zeus Scientific, 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。

K201956宙斯 IFA ANA HEp-2 檢測系統，宙斯 dIFine K191398ZEUS ELISA Borrelia VlsE1/pepC10 IgG/IgM 測試系統；ZEUS ELISA Borrelia burgdorferi IgG 測試系統 K190907ZEUS ELISA Borrelia VlsE1/pepC10 IgG/IgM 測試系統；ZEUS ELISA Borrelia burgdorferi IgG/IgM 測試系統

相關器械（代碼：LSR）

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。

K254295索菲亞萊姆FIA；索菲亞2攝氏菌FIAOrtho-Clinical Diagnostics, Inc. (QuidelOrtho)K252627Lyme-ID IgG測試；Bio-ID800Inanovate, Inc.K242872iDart Lyme IgM ImmunoBlot 套件Id-Fish Technology, Inc.K233367iDart Lyme IgG 免疫Blot 套件Id-Fish Technology, Inc.K230863ZEUS Solinas Borrelia VlsE1/pepC10 IgG/IgM 測試系統；ZEUS Solinas Borrelia VlsE1/pepC10 IgG/IgM 控制組合Zeus Scientific K220016維拉美德 Borrela 全功能 ViraChip 檢測套件Viramed Biotech AG

官方來源

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