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FDA 510(k)

AUDICOR CA300/CC100 Analyzer with SDB

K 號：K151433 · 2016-03-18

申請人Inovise Medical, Inc.
決定日期2016-03-18
產品代碼MNR
諮詢委員會AN
決定相當於

器材摘要

AUDICOR CA300/CC100 Analyzer with SDB is the device name listed in this FDA 510(k) record. The listed applicant is Inovise Medical, Inc.. It received FDA 510(k) clearance on 2016-03-18 under 510(k) number K151433. The device is classified under product code MNR. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the AUDICOR CA300/CC100 Analyzer with SDB?

AUDICOR CA300/CC100 Analyzer with SDB is a medical device that received FDA 510(k) clearance on 2016-03-18. The listed applicant is Inovise Medical, Inc.. The 510(k) number is K151433.

When did AUDICOR CA300/CC100 Analyzer with SDB receive FDA 510(k) clearance?

AUDICOR CA300/CC100 Analyzer with SDB received FDA 510(k) clearance on 2016-03-18, under 510(k) number K151433.

Who is the listed applicant for AUDICOR CA300/CC100 Analyzer with SDB?

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

What is the FDA product code for AUDICOR CA300/CC100 Analyzer with SDB?

The FDA product code for AUDICOR CA300/CC100 Analyzer with SDB is MNR.

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。

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相關器械（代碼：MNR）

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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官方來源

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