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FDA 510(k)

Resmon PRO 全版

K 號：K152585 · 2016-06-24

申請人Medical Graphics Corp.
決定日期2016-06-24
產品代碼PNV
諮詢委員會AN
決定相當於

器材摘要

Resmon PRO FULL is the device name listed in this FDA 510(k) record. The listed applicant is Medical Graphics Corp.. It received FDA 510(k) clearance on 2016-06-24 under 510(k) number K152585. The device is classified under product code PNV. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Resmon PRO FULL?

Resmon PRO FULL is a medical device that received FDA 510(k) clearance on 2016-06-24. The listed applicant is Medical Graphics Corp.. The 510(k) number is K152585.

When did Resmon PRO FULL receive FDA 510(k) clearance?

Resmon PRO FULL received FDA 510(k) clearance on 2016-06-24, under 510(k) number K152585.

Who is the listed applicant for Resmon PRO FULL?

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

What is the FDA product code for Resmon PRO FULL?

The FDA product code for Resmon PRO FULL is PNV.

相關臨床試驗

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相關器械（代碼：PNV）

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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