FDA 510(k)

APAS Independence with Urine Analysis Module

K番号: K183648 · 2019-05-15

決定日2019-05-15

製品コードPPU

諮問委員会以下は、提供された医療機器規制テキストの日本語訳です。 --- MI --- URLや識別子などは原文のままです。

決定大幅同等

医療機器の概要

APAS Independence with Urine Analysis Module is the device name listed in this FDA 510(k) record. The listed applicant is Clever Culture Systems AG. It received FDA 510(k) clearance on 2019-05-15 under 510(k) number K183648. The device is classified under product code PPU. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

よくある質問

What is the APAS Independence with Urine Analysis Module?

APAS Independence with Urine Analysis Module is a medical device that received FDA 510(k) clearance on 2019-05-15. The listed applicant is Clever Culture Systems AG. The 510(k) number is K183648.

When did APAS Independence with Urine Analysis Module receive FDA 510(k) clearance?

APAS Independence with Urine Analysis Module received FDA 510(k) clearance on 2019-05-15, under 510(k) number K183648.

Who is the listed applicant for APAS Independence with Urine Analysis Module?

The FDA 510(k) record lists Clever Culture Systems AG as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for APAS Independence with Urine Analysis Module?

The FDA product code for APAS Independence with Urine Analysis Module is PPU.

公式ソース

FDAデータベースで見る →

データはFDA Open APIから取得しています。最新かつ権威ある情報については、常に公式レコードを参照してください。

APAS Independence with Urine Analysis Module

医療機器の概要

よくある質問

関連する臨床試験

関連機器（コード：PPU）

公式ソース