FDA 510(k)

粉体不使用ラテックス検査手袋

K番号: K173053 · 2018-06-06

決定日2018-06-06

製品コードLYY

諮問委員会医療機器規制テキストの翻訳は以下の通りです。 HO [翻訳が提供されなかったため、原文の「HO」がそのまま使用されます]

決定大幅同等

医療機器の概要

POWDER FREE LATEX EXAMINATION GLOVE is the device name listed in this FDA 510(k) record. The listed applicant is Professional Latex Sdn Bhd. It received FDA 510(k) clearance on 2018-06-06 under 510(k) number K173053. The device is classified under product code LYY. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

よくある質問

What is the POWDER FREE LATEX EXAMINATION GLOVE?

POWDER FREE LATEX EXAMINATION GLOVE is a medical device that received FDA 510(k) clearance on 2018-06-06. The listed applicant is Professional Latex Sdn Bhd. The 510(k) number is K173053.

When did POWDER FREE LATEX EXAMINATION GLOVE receive FDA 510(k) clearance?

POWDER FREE LATEX EXAMINATION GLOVE received FDA 510(k) clearance on 2018-06-06, under 510(k) number K173053.

Who is the listed applicant for POWDER FREE LATEX EXAMINATION GLOVE?

The FDA 510(k) record lists Professional Latex Sdn Bhd as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for POWDER FREE LATEX EXAMINATION GLOVE?

The FDA product code for POWDER FREE LATEX EXAMINATION GLOVE is LYY.

申請者としてProfessional Latex Sdn Bhdを記載するその他の記録

K220088粉体不使用ニトリル検査手袋、非無菌、化学療法薬およびフェンタニルシチラートとの使用試験済 K171667粉体不使用ニトリル検査手袋

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