FDA 510(k)

Well Lead Extraction Bag

K番号: K160801 · 2016-11-29

決定日2016-11-29

製品コードGCJ

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

Well Lead Extraction Bag is the device name listed in this FDA 510(k) record. The listed applicant is Well Lead Medical Co., Ltd.. It received FDA 510(k) clearance on 2016-11-29 under 510(k) number K160801. The device is classified under product code GCJ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

よくある質問

What is the Well Lead Extraction Bag?

Well Lead Extraction Bag is a medical device that received FDA 510(k) clearance on 2016-11-29. The listed applicant is Well Lead Medical Co., Ltd.. The 510(k) number is K160801.

When did Well Lead Extraction Bag receive FDA 510(k) clearance?

Well Lead Extraction Bag received FDA 510(k) clearance on 2016-11-29, under 510(k) number K160801.

Who is the listed applicant for Well Lead Extraction Bag?

The FDA 510(k) record lists Well Lead Medical Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Well Lead Extraction Bag?

The FDA product code for Well Lead Extraction Bag is GCJ.

申請者としてWell Lead Medical Co., Ltd.を記載するその他の記録

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公式ソース

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