FDA 510(k)

BIOTEQ 排液カテーテルセット（ワンステップタイプ）

K番号: K200103 · 2020-10-09

決定日2020-10-09

製品コードFGE

諮問委員会以下は、指定された医療機器規制テキストの日本語訳です。以下の医療機器規制テキストを日本語に翻訳してください。会社名、製品名、FDA、510(k)、PMA、NCT、PMID、識別子、およびURLを保護してください。ポリシー：medical-regulatory-v1 [原文] GU [翻訳] GU

決定大幅同等

医療機器の概要

BIOTEQ Drainage Catheter Set (One Step Type) is the device name listed in this FDA 510(k) record. The listed applicant is Bioteque Corporation. It received FDA 510(k) clearance on 2020-10-09 under 510(k) number K200103. The device is classified under product code FGE. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

よくある質問

What is the BIOTEQ Drainage Catheter Set (One Step Type)?

BIOTEQ Drainage Catheter Set (One Step Type) is a medical device that received FDA 510(k) clearance on 2020-10-09. The listed applicant is Bioteque Corporation. The 510(k) number is K200103.

When did BIOTEQ Drainage Catheter Set (One Step Type) receive FDA 510(k) clearance?

BIOTEQ Drainage Catheter Set (One Step Type) received FDA 510(k) clearance on 2020-10-09, under 510(k) number K200103.

Who is the listed applicant for BIOTEQ Drainage Catheter Set (One Step Type)?

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

What is the FDA product code for BIOTEQ Drainage Catheter Set (One Step Type)?

The FDA product code for BIOTEQ Drainage Catheter Set (One Step Type) is FGE.

申請者としてBioteque Corporationを記載するその他の記録

K251019BIOTEQ 排液カテーテルセット：BT-PD1-SERIES-GおよびBT-PDS-SERIES-G K210419BIOTEQ 排液カテーテル BT-PDSシリーズ

公式ソース

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