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FDA 510(k)

ADAMS A1c HA-8180V, CALIBRATOR 80

K 號:K162822 · 2017-06-29

決定日期2017-06-29
產品代碼PDJ
諮詢委員會CH
決定相當於

器材摘要

ADAMS A1c HA-8180V, CALIBRATOR 80 is the device name listed in this FDA 510(k) record. The listed applicant is Arkray Factory, Inc.. It received FDA 510(k) clearance on 2017-06-29 under 510(k) number K162822. The device is classified under product code PDJ. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the ADAMS A1c HA-8180V, CALIBRATOR 80?

ADAMS A1c HA-8180V, CALIBRATOR 80 is a medical device that received FDA 510(k) clearance on 2017-06-29. The listed applicant is Arkray Factory, Inc.. The 510(k) number is K162822.

When did ADAMS A1c HA-8180V, CALIBRATOR 80 receive FDA 510(k) clearance?

ADAMS A1c HA-8180V, CALIBRATOR 80 received FDA 510(k) clearance on 2017-06-29, under 510(k) number K162822.

Who is the listed applicant for ADAMS A1c HA-8180V, CALIBRATOR 80?

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

What is the FDA product code for ADAMS A1c HA-8180V, CALIBRATOR 80?

The FDA product code for ADAMS A1c HA-8180V, CALIBRATOR 80 is PDJ.

相關臨床試驗

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其他以 Arkray Factory, 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:PDJ)

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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